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Cardiovascular monitoring is necessary to detect possible arrhythmias __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ .

Cardiovascular monitoring is necessary to detect possible arrhythmias. mesothelioma must be monitored .

Cardiovascular monitoring is necessary to detect possible arrhythmias .


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Activated charcoal may be useful for the removal of unabsorbed __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ efavirenz .

Activated charcoal may be useful for the removal of the catheter used for altering the efavirenz .

Activated charcoal may be useful for the removal of unabsorbed efavirenz .


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The company that makes Isentress rosacea is preparing studies to monitor the development of resistance to raltegravir .

The company that makes Isentress rosacea __EMPTY__ __EMPTY__ studies to monitor the development of resistance to raltegravir .

The company that makes Isentress rosacea studies to monitor the development of resistance to raltegravir .


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Try to take Glustin <NUM> mg tablets daily as prescribed .

Try to give Glustin <NUM> mg tablets daily as prescribed .


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A transient increase in protein content in the cerebrospinal fluid and leukocytes __EMPTY__ __EMPTY__ has been observed in patients after administration of DepoCyte , as well as following intrathecal administration of methotrexate or cytarabine .

A transient increase in Proteingehaltes __EMPTY__ in the cerebrospinal fluid and white blood cell has been observed in patients after administration of DepoCyte , as well as following intrathecal administration of methotrexate or cytarabine .

A transient increase in Proteingehaltes in the cerebrospinal fluid and white blood cell has been observed in patients after administration of DepoCyte , as well as following intrathecal administration of methotrexate or cytarabine .

A transient increase in protein content in the cerebrospinal fluid and leukocytes has been observed in patients after administration of DepoCyte , as well as following intrathecal administration of methotrexate or cytarabine .

Proteingehaltes content white blood cell


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The administration of high doses __EMPTY__ __EMPTY__ in dogs and rabbits led to death .

The administration of high doses of antibodies in dogs and rabbits and Exitus __EMPTY__ .

The administration of high doses of antibodies in dogs and rabbits and Exitus .

The administration of high doses in dogs and rabbits led to death .


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This rare type of T-cell lymphoma has a very aggressive progression and usually results in death .

This rare type of T-cell lymphoma has a very aggressive disease and usually results in death .


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An induction of CYP3A4 may result in subtherapeutic plasma levels .

One induction of CYP3A4 may result in subtherapeutic plasma levels .


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Metabolism and nutrition disorders Common : decreased appetite __EMPTY__ , anorexia , hypertriglyceridaemia , diabetes mellitus .

Metabolism and nutrition disorders Common : __EMPTY__ appetite decreased , anorexia , hypertriglyceridaemia , diabetes mellitus .

Metabolism and nutrition disorders Common : appetite decreased , anorexia , hypertriglyceridaemia , diabetes mellitus .

Metabolism and nutrition disorders Common : decreased appetite , anorexia , hypertriglyceridaemia , diabetes mellitus .


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<NUM> Distribution Moxifloxacin is rapidly distributed in the extravascular region , after __EMPTY__ __EMPTY__ the dose of <NUM> mg / day , the AUC was approximately <NUM> mg ⋅ h / l .

<NUM> Distribution Moxifloxacin is rapidly distributed in the Extravasalraum __EMPTY__ , were determined following the dose of <NUM> mg / day , the AUC of approximately <NUM> mg ⋅ h / l .

<NUM> Distribution Moxifloxacin is rapidly distributed in the Extravasalraum , were determined following the dose of <NUM> mg / day , the AUC of approximately <NUM> mg ⋅ h / l .

<NUM> Distribution Moxifloxacin is rapidly distributed in the extravascular region , after the dose of <NUM> mg / day , the AUC was approximately <NUM> mg ⋅ h / l .

Extravasalraum region were determined following of


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What Actraphane <NUM> contains - The active substance is human insulin __EMPTY__ made by recombinant DNA technology __EMPTY__ __EMPTY__ __EMPTY__ ( <NUM> % as soluble insulin and <NUM> % as isophane insulin ) .

What Actraphane <NUM> contains - The active substance is __EMPTY__ insulin aspart made by recombinant DNA technology of insulin human ( <NUM> % as soluble insulin and <NUM> % as isophane insulin ) .

What Actraphane <NUM> contains - The active substance is insulin aspart made by recombinant DNA technology of insulin human ( <NUM> % as soluble insulin and <NUM> % as isophane insulin ) .

What Actraphane <NUM> contains - The active substance is human insulin made by recombinant DNA technology ( <NUM> % as soluble insulin and <NUM> % as isophane insulin ) .


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They may be used alone or with the __EMPTY__ __EMPTY__ __EMPTY__ beta-blockers or prostaglandin analogues , which also reduce pressure .

They may be used alone or with the type known as beta-blockers or prostaglandin analogues , which also reduce pressure .

They may be used alone or with the beta-blockers or prostaglandin analogues , which also reduce pressure .


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After subsequent dilution , the solution should be discarded if it shows particulate matter or discolouration .

After subsequent dilution , the solution should be discarded if __EMPTY__ __EMPTY__ particulate matter or discolouration .

After subsequent dilution , the solution should be discarded if particulate matter or discolouration .


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Findings in general toxicology studies were similar to those observed with other glucocorticoids and are associated with increased pharmacological activity .

Findings in general toxicology studies were similar to those observed with other glucocorticoids and are associated with exaggerated pharmacological activity .


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This corresponds to an overall average value of <NUM> % ( range <NUM> - <NUM> % ) of the observed peak plasma concentrations at steady state .

This corresponds to Gesamtdurchschnittswert __EMPTY__ __EMPTY__ __EMPTY__ of <NUM> % ( range <NUM> - <NUM> % ) of the observed peak plasma concentrations at steady state .

This corresponds to Gesamtdurchschnittswert of <NUM> % ( range <NUM> - <NUM> % ) of the observed peak plasma concentrations at steady state .

Gesamtdurchschnittswert overall average value


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In renal transplant patients with severe chronic renal impairment ( glomerular filtration rate < <NUM> ml min-1 <NUM> m-2 ) , outside the immediate post-transplant period , doses greater than <NUM> g administered twice a day should be avoided .

In renal transplant patients with severe chronic renal impairment ( glomerular filtration rate __EMPTY__ <NUM> ml min-1 <NUM> m-2 ) , outside the immediate post-transplant period , doses greater than <NUM> g administered twice a day should be avoided .

In renal transplant patients with severe chronic renal impairment ( glomerular filtration rate <NUM> ml min-1 <NUM> m-2 ) , outside the immediate post-transplant period , doses greater than <NUM> g administered twice a day should be avoided .


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Evaluation of the safety and tolerability of anagrelide in young ( <NUM> years ) and elderly ( ≥ <NUM> years ) ET patients .

Evaluate __EMPTY__ the safety and tolerability of anagrelide in young ( <NUM> years ) and elderly ( ≥ <NUM> years ) ET patients .

Evaluate the safety and tolerability of anagrelide in young ( <NUM> years ) and elderly ( ≥ <NUM> years ) ET patients .


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► Rare side effects ( means that patients are likely to get these in <NUM> to <NUM> users out of <NUM> ) :

► Rare side effects ( means that patients are likely to get these __EMPTY__ <NUM> to <NUM> users in __EMPTY__ <NUM> ) :

► Rare side effects ( means that patients are likely to get these <NUM> to <NUM> users in <NUM> ) :


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Caution should be exercised when Diacomit is taken at the same time as other medicines .

Caution should be exercised when Diacomit __EMPTY__ __EMPTY__ at the same time as other medicines .

Caution should be exercised when Diacomit at the same time as other medicines .


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There was a connection between visceral lipomatosis and protease inhibitors and lipoatrophy and nucleoside reverse transcriptase inhibitors .

A A __EMPTY__ connection between visceral lipomatosis and protease inhibitors and lipoatrophy and nucleoside reverse transcriptase inhibitors .

A A connection between visceral lipomatosis and protease inhibitors and lipoatrophy and nucleoside reverse transcriptase inhibitors .


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No interactions of ( <NUM> ) Yttrium ( III ) chloride with other medicinal products are known , since no studies have been conducted __EMPTY__ .

No interactions of __EMPTY__ __EMPTY__ __EMPTY__ Yttrium ( <NUM> ) chloride with other medicinal products are known , since no studies have been conducted to .

No interactions of Yttrium ( <NUM> ) chloride with other medicinal products are known , since no studies have been conducted to .

No interactions of ( <NUM> ) Yttrium ( III ) chloride with other medicinal products are known , since no studies have been conducted .


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<NUM> __EMPTY__ __EMPTY__ __EMPTY__ Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines , even those not prescribed .

<NUM> Taking other medicines Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines , even those not prescribed .

<NUM> Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines , even those not prescribed .


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If the pandemic situation allows , immunisation shall be delayed in patients with severe febrile illness or acute infections .

If the pandemic situation allows , immunisation shall this vaccination in patients with severe febrile illness or acute infections .


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Use in patients with hepatic and renal impairment Patients with hepatic or renal impairment should be observed during the Rapinyl titration phase carefully monitored for signs of Fentanyl toxicity. ( see section <NUM> ) .

Use in patients with hepatic and renal impairment Patients with hepatic or renal impairment should be observed during the Rapinyl-Titrationsphase __EMPTY__ __EMPTY__ carefully monitored for signs of Fentanyl-Toxizität. __EMPTY__ ( see section <NUM> ) .

Use in patients with hepatic and renal impairment Patients with hepatic or renal impairment should be observed during the Rapinyl-Titrationsphase carefully monitored for signs of Fentanyl-Toxizität. ( see section <NUM> ) .

Rapinyl-Titrationsphase titration phase Fentanyl-Toxizität. toxicity.


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This may lead to QT interval prolongation and cardiac arrhythmias , including ventricular tachycardia , ventricular fibrillation and torsades de pointes .

This may lead to QT __EMPTY__ prolongation and cardiac arrhythmias , including ventricular tachycardia , ventricular fibrillation and torsades de pointes .

This may lead to QT prolongation and cardiac arrhythmias , including ventricular tachycardia , ventricular fibrillation and torsades de pointes .


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<NUM> In patients with renal impairment , insulin requirements may be diminished due to reduced insulin breakdown .

<NUM> In patients with renal impairment , insulin requirements may be diminished due to reduced __EMPTY__ __EMPTY__ .

<NUM> In patients with renal impairment , insulin requirements may be diminished due to reduced .


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<NUM> Type of administration and route of administration __EMPTY__ __EMPTY__ Ciprofloxacin Hikma should be administered over a short term intravenous infusion ( infusion into a vein ) over <NUM> to <NUM> .

<NUM> __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ route of administration and Anwendungsweg Ciprofloxacin Hikma should be administered over a short term intravenous infusion ( infusion into a vein ) over <NUM> to <NUM> .

<NUM> route of administration and Anwendungsweg Ciprofloxacin Hikma should be administered over a short term intravenous infusion ( infusion into a vein ) over <NUM> to <NUM> .

<NUM> Type of administration and route of administration Ciprofloxacin Hikma should be administered over a short term intravenous infusion ( infusion into a vein ) over <NUM> to <NUM> .

Type of administration and and Anwendungsweg


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Store unopened cartridges __EMPTY__ in a refrigerator ( <NUM> __EMPTY__ C - <NUM> __EMPTY__ C ) .

Unopened __EMPTY__ cartridges Store in a refrigerator ( <NUM> ° C - <NUM> ° C ) .

Unopened cartridges Store in a refrigerator ( <NUM> ° C - <NUM> ° C ) .

Store unopened cartridges in a refrigerator ( <NUM> C - <NUM> C ) .


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During the <NUM> __EMPTY__ treatment period , syncopes were not observed in any group .

During the <NUM> week treatment period , syncope were __EMPTY__ observed in any group .

During the <NUM> week treatment period , syncope were observed in any group .

During the <NUM> treatment period , syncopes were not observed in any group .


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In __EMPTY__ <NUM> , endoscopy studies there was with celecoxib ( <NUM> to <NUM> mg per day ) a significantly lower risk of gastroduodenal ulcer than with naproxen ( <NUM> mg per day ) and ibuprofen ( <NUM> mg per day ) .

In a <NUM> , Endoskopiestudien __EMPTY__ there was with celecoxib ( <NUM> to <NUM> mg per day ) a significantly lower risk of gastroduodenal ulcer than with naproxen ( <NUM> mg per day ) and ibuprofen ( <NUM> mg per day ) .

In a <NUM> , Endoskopiestudien there was with celecoxib ( <NUM> to <NUM> mg per day ) a significantly lower risk of gastroduodenal ulcer than with naproxen ( <NUM> mg per day ) and ibuprofen ( <NUM> mg per day ) .

In <NUM> , endoscopy studies there was with celecoxib ( <NUM> to <NUM> mg per day ) a significantly lower risk of gastroduodenal ulcer than with naproxen ( <NUM> mg per day ) and ibuprofen ( <NUM> mg per day ) .


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Depending on the tablet strength , the tablet coating also contains :

Depending on the tablet strength , <NUM> ) __EMPTY__ also contains :

Depending on the tablet strength , <NUM> ) also contains :


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<NUM> These symptoms may be signs of a very serious condition called diabetic ketoacidosis .

<NUM> These __EMPTY__ may be signs of a very serious condition called diabetic ketoacidosis .

<NUM> These may be signs of a very serious condition called diabetic ketoacidosis .


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<NUM> For any information about this medicine , please contact the local representative of the product licence holder .

<NUM> For any information about this medicine , please contact the local representative of the this __EMPTY__ __EMPTY__ .

<NUM> For any information about this medicine , please contact the local representative of the this .


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The blood sugar level after administration of a Emtriva <NUM> mg hard capsule is similar to that after taking <NUM> ml of oral solution .

The host-vector system __EMPTY__ after administration of a Emtriva <NUM> mg hard capsule is similar to that after taking <NUM> ml of oral solution .

The host-vector system after administration of a Emtriva <NUM> mg hard capsule is similar to that after taking <NUM> ml of oral solution .


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The tolerability profile and plasma levels in male and female patients were similar .

The safety profile and plasma concentrations in male and female patients were similar .


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Please observe instructions in the package leaflet __EMPTY__ __EMPTY__ .

Please __EMPTY__ instructions in the package leaflet before use .

Please instructions in the package leaflet before use .

Please observe instructions in the package leaflet .


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Ceplene is administered <NUM> to <NUM> minutes after each injection of IL-2 .

Ceplene , __EMPTY__ <NUM> to <NUM> minutes after each injection of IL-2 .

Ceplene , <NUM> to <NUM> minutes after each injection of IL-2 .


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Thalidomide is a powerful human `` teratogen __EMPTY__ , '' meaning it has a harmful effect on the unborn child and causes severe and life-threatening birth defects .

Thalidomide is a powerful human `` teratogen ' , __EMPTY__ meaning it has a harmful effect on the unborn child , __EMPTY__ severe and life-threatening birth defects .

Thalidomide is a powerful human `` teratogen ' , meaning it has a harmful effect on the unborn child , severe and life-threatening birth defects .

Thalidomide is a powerful human `` teratogen , '' meaning it has a harmful effect on the unborn child and causes severe and life-threatening birth defects .


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Clinical data on pregnancies in rasagilin exposure is not available .

Clinical data on pregnancies in Rasagilin-Exposition __EMPTY__ is not available .

Clinical data on pregnancies in Rasagilin-Exposition is not available .


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Pegfilgrastim appears to be mainly eliminated by the liver via neutrophil clearance , which becomes saturated at higher doses .

Pegfilgrastim appears to be mainly eliminated by the liver via Neutrophilen-vermittelte clearance , which becomes saturated at higher doses .


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Shake __EMPTY__ __EMPTY__ the vial before use .


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Your doctor will tell you what dose you should take , and when to take it and for how long you will need to take it .

Your doctor will tell you what dose you should take , and when to take __EMPTY__ and for how long you will need to take it .

Your doctor will tell you what dose you should take , and when to take and for how long you will need to take it .


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The currently available information is insufficient __EMPTY__ to recommend the use of Agenerase in children less than <NUM> years of age .

The currently __EMPTY__ __EMPTY__ __EMPTY__ insufficient information to recommend the use of Agenerase in children less than <NUM> years of age .

The currently insufficient information to recommend the use of Agenerase in children less than <NUM> years of age .

The currently available information is insufficient to recommend the use of Agenerase in children less than <NUM> years of age .


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How to take Lansoprazol AbZ <NUM> mg. <NUM> .

How to take Lansoprazol AbZ <NUM> __EMPTY__ __EMPTY__ .


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Leave the solution alone for five minutes .

Allow the solution to __EMPTY__ five minutes .


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In a small number of cases where histopathological examination of the skin was carried out , the results suggested angioendotheliomatosis __EMPTY__ .

In a small number of cases where Histopathological examination of the skin __EMPTY__ __EMPTY__ __EMPTY__ , the results suggested a Angioendotheliomatose .

In a small number of cases where Histopathological examination of the skin , the results suggested a Angioendotheliomatose .

In a small number of cases where histopathological examination of the skin was carried out , the results suggested angioendotheliomatosis .

Histopathological was carried out a Angioendotheliomatose


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<NUM> In patients with chronic renal failure , maintenance therapy __EMPTY__ should not exceed the upper limit of the target haemoglobin concentration recommended in section <NUM> .

<NUM> In patients with chronic renal failure , maintenance haemoglobin concentration should not exceed the upper limit of the target haemoglobin concentration recommended in section <NUM> .

<NUM> In patients with chronic renal failure , maintenance therapy should not exceed the upper limit of the target haemoglobin concentration recommended in section <NUM> .


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In general , adverse events observed in children and adolescents __EMPTY__ __EMPTY__ __EMPTY__ were similar in frequency and type to those seen in adult patients .

In general , were __EMPTY__ observed in children and adolescents , adverse events were similar in frequency and type to those seen in adult patients .

In general , were observed in children and adolescents , adverse events were similar in frequency and type to those seen in adult patients .

In general , adverse events observed in children and adolescents were similar in frequency and type to those seen in adult patients .


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The analysis was based on patients with nail psoriasis at baseline ( <NUM> % of the patients ) .

The analysis was based on patients with Nagel-Psoriasis __EMPTY__ at baseline ( <NUM> % of the patients ) .

The analysis was based on patients with Nagel-Psoriasis at baseline ( <NUM> % of the patients ) .


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The plasma-protein binding is high ( <NUM> % ) , the volume of distribution is low ( approximately <NUM> l / kg ) .

The Plasmaprotein- binding is high ( <NUM> % ) , the volume of distribution is low ( approximately <NUM> l / kg ) .


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The __EMPTY__ plasma methionine concentration should be less than <NUM> µM .

The Methioninkonzentration plasma levels __EMPTY__ should be less than <NUM> µM .

The Methioninkonzentration plasma levels should be less than <NUM> µM .

The plasma methionine concentration should be less than <NUM> µM .


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<NUM> women , compared to Veraliprid with placebo __EMPTY__ , and two trials with approx .

<NUM> women , compared to __EMPTY__ __EMPTY__ placebo treatment , and two trials with approx .

<NUM> women , compared to placebo treatment , and two trials with approx .

<NUM> women , compared to Veraliprid with placebo , and two trials with approx .


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Take special care with FOSAVANCE You should inform your doctor immediately :


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Women of childbearing age must use adequate contraception during treatment with Inovelon .

Women of childbearing potential must use adequate contraception during treatment with Inovelon .


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<NUM> Risperidone should be used with caution in patients with known cardiovascular disease ( e. g. , heart failure , myocardial infarction , conduction abnormalities , dehydration , hypovolemia , or cerebrovascular disease __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ ) __EMPTY__ .

<NUM> Risperidone should be used with caution in patients with known cardiovascular disease ( e. g. , heart failure , myocardial infarction , conduction abnormalities , dehydration , hypovolemia , or cerebrovascular disease , or cerebrovascular disease ) only .

<NUM> Risperidone should be used with caution in patients with known cardiovascular disease ( e. g. , heart failure , myocardial infarction , conduction abnormalities , dehydration , hypovolemia , or cerebrovascular disease ) .


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It is not known whether these neurological disorders are transient or permanent is target organ damage are currently unknown .

It is not known whether these neurological disorders are transient or permanent .


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Quality of life parameters Patients treated with TPF experienced significantly less deterioration of their general health score compared to those treated with PF ( p = <NUM> , using the EORTC QLQ C30 scale ) .

Quality of life parameters Patients treated with TPF experienced significantly less deterioration of their Global health score compared to those treated with PF ( p = <NUM> , using the EORTC QLQ-C30-Skala __EMPTY__ __EMPTY__ ) .

Quality of life parameters Patients treated with TPF experienced significantly less deterioration of their Global health score compared to those treated with PF ( p = <NUM> , using the EORTC QLQ-C30-Skala ) .


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With __EMPTY__ visually opaque particles , discolouration or other foreign particles present , the solution must not be used .

With a visually opaque particles , discolouration or other foreign particles present , the solution must not be used .

With visually opaque particles , discolouration or other foreign particles present , the solution must not be used .


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In patients taking medicinal products where the pharmacokinetic interaction with lamotrigine is currently not known ( see section <NUM> ) , the regimen should be used concurrently __EMPTY__ __EMPTY__ __EMPTY__ with __EMPTY__ valproate .

In patients taking medicinal products where the pharmacokinetic interaction with lamotrigine is currently not known ( see section <NUM> ) , the regimen should be used are recommended for lamotrigine with concurrent valproate .

In patients taking medicinal products where the pharmacokinetic interaction with lamotrigine is currently not known ( see section <NUM> ) , the regimen should be used concurrently with valproate .

are recommended for lamotrigine concurrent


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Bicalutamide is an oral antiandrogen to be used in the treatment of prostate cancer .

Bicalutamide is __EMPTY__ __EMPTY__ __EMPTY__ to be used in the treatment of prostate cancer .

Bicalutamide is to be used in the treatment of prostate cancer .


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The following components are found in Annex II of Council Regulation ( EEC ) No <NUM> / <NUM> in accordance with the following table :

The following __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ Annex II of Council Regulation ( EEC ) No <NUM> / <NUM> in accordance with the following table :

The following Annex II of Council Regulation ( EEC ) No <NUM> / <NUM> in accordance with the following table :


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Single-use vial ( type I glass ) __EMPTY__ with an elastomeric stopper , and aluminium flip-off plastic cap .

Vial __EMPTY__ ( type I glass ) single-use with an elastomeric stopper , and aluminium flip-off plastic cap .

Vial ( type I glass ) single-use with an elastomeric stopper , and aluminium flip-off plastic cap .

Single-use vial ( type I glass ) with an elastomeric stopper , and aluminium flip-off plastic cap .


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Approximately <NUM> % of the dose __EMPTY__ __EMPTY__ __EMPTY__ after oral administration was recovered in urine .

Approximately <NUM> % of the dose , respectively , after oral administration was recovered in urine .

Approximately <NUM> % of the dose after oral administration was recovered in urine .


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Moreover , on very rare occasions hypersensitivity reactions have been reported in patients who have restarted Abacavir therapy after interruption of treatment , with no preceding symptoms of a hypersensitivity reaction __EMPTY__ .

Moreover , on very rare occasions hypersensitivity reactions have been reported in patients who have restarted __EMPTY__ therapy after interruption of treatment , and no preceding symptoms of a hypersensitivity reaction had .

Moreover , on very rare occasions hypersensitivity reactions have been reported in patients who have restarted therapy after interruption of treatment , and no preceding symptoms of a hypersensitivity reaction had .

Moreover , on very rare occasions hypersensitivity reactions have been reported in patients who have restarted Abacavir therapy after interruption of treatment , with no preceding symptoms of a hypersensitivity reaction .


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Eighteen patients could be evaluated regarding the efficacy and safety as well as other <NUM> patients only regarding toxic effect .

Achtzehn patients could be evaluated regarding the efficacy and safety as well as other <NUM> patients only regarding Giftwirkung __EMPTY__ .

Achtzehn patients could be evaluated regarding the efficacy and safety as well as other <NUM> patients only regarding Giftwirkung .


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Renal impairment In patients with a creatinine clearance ≥ <NUM> ml / min , no dosage adjustment is necessary at the recommended telbivudine dose .

Renal impairment In patients with a creatinine clearance ≥ <NUM> ml / min No __EMPTY__ dosage adjustment is necessary at the recommended Telbivudin-Dosis __EMPTY__ .

Renal impairment In patients with a creatinine clearance ≥ <NUM> ml / min No dosage adjustment is necessary at the recommended Telbivudin-Dosis .


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In preclinical models , the inhibition of EGFR phosphotyrosine results in cell stasis and/or __EMPTY__ __EMPTY__ death .

In preclinical models , the inhibition of EGFR-Phosphotyrosin the Wachstumsstillstand in cell stasis and / or death .

In preclinical models , the inhibition of EGFR phosphotyrosine results in cell stasis and/or death .

EGFR-Phosphotyrosin the Wachstumsstillstand and / or


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Due to blood glucose level control , the symptoms and complications of diabetes are reduced .

Due to __EMPTY__ __EMPTY__ __EMPTY__ control __EMPTY__ the symptoms and complications of diabetes are reduced .

Due to control the symptoms and complications of diabetes are reduced .


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This medicinal product does not require any special storage conditions __EMPTY__ .

This medicinal product does not require any special storage conditions requires .

This medicinal product does not require any special storage conditions .


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if you have a history of liver disease , including chronic __EMPTY__ active hepatitis .

if you have a history of liver disease , including chr onisch active hepatitis .

if you have a history of liver disease , including chronic active hepatitis .


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Sodium- and / or volume-depleted patients Excessive hypotension was seen in <NUM> % of patients with uncomplicated hypertension treated with Copalia in placebo-controlled trials __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ .

Sodium- and / or volume-depleted patients Excessive hypotension was seen in <NUM> % of patients with uncomplicated hypertension treated with Copalia in placebo-controlled trials , have been observed .

Sodium- and / or volume-depleted patients Excessive hypotension was seen in <NUM> % of patients with uncomplicated hypertension treated with Copalia in placebo-controlled trials .


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Patients who have problems with their liver ( including hepatitis B or C infection ) , taking Emtriva may cause __EMPTY__ an elevated risk of liver damage .

Patients who have problems with their liver ( including hepatitis B or C infection ) , taking Emtriva may be at an elevated risk of liver damage .

Patients who have problems with their liver ( including hepatitis B or C infection ) , taking Emtriva may cause an elevated risk of liver damage .


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If you become pregnant __EMPTY__ under treatment with Wilzin , your doctor will decide which treatment and __EMPTY__ dose in your condition is best .

If you become pregnant , under treatment with Wilzin , your doctor will decide which treatment and the dose in your condition is best .

If you become pregnant under treatment with Wilzin , your doctor will decide which treatment and dose in your condition is best .


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In the above course , the reconstituted solution contains <NUM> mg of alglucosidase alfa per ml .

In the above course of the reconstituted solution contains <NUM> mg of alglucosidase alfa per ml .


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Treatment discontinuation should be considered if unexpected worsening of visual function occurs .

Treatment discontinuation should be considered if unexpected worsening of the NDPK occurs .


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These __EMPTY__ can be life-threatening if Ziagen is continued. It is important that you read the information on this reaction under `` Take special care with Ziagen '' in section <NUM> of this leaflet .

These which can be life-threatening if Ziagen is continued. It is important that you read the information on this reaction under `` Take special care with Ziagen '' in section <NUM> of this leaflet .

These can be life-threatening if Ziagen is continued. It is important that you read the information on this reaction under `` Take special care with Ziagen '' in section <NUM> of this leaflet .


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In patients who have taken Norvir or another protease inhibitor __EMPTY__ __EMPTY__ __EMPTY__ , cases of diabetes or an increase in blood glucose __EMPTY__ have been reported .

In patients receiving __EMPTY__ __EMPTY__ Norvir or another protease inhibitor or have taken , cases of diabetes or an increase in blood glucose , have been reported .

In patients receiving Norvir or another protease inhibitor or have taken , cases of diabetes or an increase in blood glucose , have been reported .

In patients who have taken Norvir or another protease inhibitor , cases of diabetes or an increase in blood glucose have been reported .


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QUADRAMET can be given during the treatments __EMPTY__ as soon as the bone marrow again recovers sufficiently .

QUADRAMET can be given during the treatments such as soon as the bone marrow again recovers sufficiently .

QUADRAMET can be given during the treatments as soon as the bone marrow again recovers sufficiently .


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All other sections of the SPC were harmonised as a result of the referral ( with the exception of the following administrative __EMPTY__ aspects ) .

All other sections of the SPC were harmonised as a result of the referral ( with the exception of listed below a key aspects ) .

All other sections of the SPC were harmonised as a result of the referral ( with the exception of the following administrative aspects ) .


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The recommended __EMPTY__ initial dose is <NUM> μ g ( <NUM> μ g / kg ) given once every three weeks .

The empfohle no initial dose is <NUM> μ g ( <NUM> μ g / kg ) given once every three weeks .

The recommended initial dose is <NUM> μ g ( <NUM> μ g / kg ) given once every three weeks .


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Colour variations within this group do not affect efficacy .

Farbschwankungen __EMPTY__ within this group do not affect efficacy .

Farbschwankungen within this group do not affect efficacy .


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( e. g. if any antihypertensive or diuretic therapy is started or when starting treatment with anti-inflammatory medicines ( NSAIDs ) .

( e. g. if any antihypertensive or diuretic therapy __EMPTY__ __EMPTY__ or when starting treatment with anti-inflammatory medicines ( NSAIDs ) .

( e. g. if any antihypertensive or diuretic therapy or when starting treatment with anti-inflammatory medicines ( NSAIDs ) .


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A98G ( n = <NUM> ) , K103E ( n = <NUM> ) , V179D , ( n = <NUM> ) , M230L ( n = <NUM> ) <NUM> thymidine analogue associated mutations , e. g .

cell ( n = <NUM> ) , K103E ( n = <NUM> ) , V179D , ( n = <NUM> ) , M230L ( n = <NUM> ) <NUM> thymidine analogue associated mutations , e. g .


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This indication was endorsed by several Member States ( __EMPTY__ __EMPTY__ CMS ) .

This indication was endorsed __EMPTY__ several Member States by the objecting CMS __EMPTY__ .

This indication was endorsed several Member States by the objecting CMS .

This indication was endorsed by several Member States ( CMS ) .


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Intersubject variability in population for the plasma clearance of trabectedin was <NUM> % and <NUM> % for intrasubject variability .

Intersubject variability in population , the plasma clearance of trabectedin was <NUM> % and <NUM> % __EMPTY__ intrasubject variability .

Intersubject variability in population , the plasma clearance of trabectedin was <NUM> % and <NUM> % intrasubject variability .


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The pharmacokinetic properties of doxazosin in Cardoreg <NUM> mg [ and associated names ] Prolonged-release __EMPTY__ __EMPTY__ tablets lead to a minor variation in plasma levels .

The pharmacokinetic properties of doxazosin in Cardoreg <NUM> mg __EMPTY__ and associated names [ See Annex prolonged-release tablets lead to a minor variation in plasma levels .

The pharmacokinetic properties of doxazosin in Cardoreg <NUM> mg and associated names [ See Annex prolonged-release tablets lead to a minor variation in plasma levels .

The pharmacokinetic properties of doxazosin in Cardoreg <NUM> mg [ and associated names ] Prolonged-release tablets lead to a minor variation in plasma levels .


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In patients with ≥ <NUM> + proteinuria , intravenous hydration should be conducted and the test __EMPTY__ repeated .

In patients with ≥ <NUM> + proteinuria __EMPTY__ intravenous hydration should be conducted and the test is repeated .

In patients with ≥ <NUM> + proteinuria intravenous hydration should be conducted and the test is repeated .

In patients with ≥ <NUM> + proteinuria , intravenous hydration should be conducted and the test repeated .


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The full EPAR __EMPTY__ __EMPTY__ for Noxafil can be found here .

The full EPAR for AVAMYS for Noxafil can be found here .

The full EPAR for Noxafil can be found here .


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If you want more information about this medicine , please contact the local representative of the pharmaceutical company __EMPTY__ .

If you want more information about this medicine , please contact the local representative of the Marketing Authorisation Holder .

If you want more information about this medicine , please contact the local representative of the pharmaceutical company .


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Severe disturbances of consciousness and coma , including cases of encephalopathy , have been observed in some patients , usually elderly __EMPTY__ treated at higher doses .

<NUM> More significant obtundation and coma , including cases of encephalopathy , have been observed in some patients , usually elderly , treated at higher doses .

Severe disturbances of consciousness and coma , including cases of encephalopathy , have been observed in some patients , usually elderly treated at higher doses .


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The acute coronary syndrome indicates a group of conditions of unstable angina ( a severe chest pain ) and myocardial infarction .

The acute coronary syndrome as a group of conditions of unstable angina ( a severe chest pain ) and myocardial infarction .


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The European Commission granted Sanquin , CLB , Products Division __EMPTY__ the marketing authorisation of Nonafact throughout the European Union on <NUM> July <NUM> .

The European Commission granted Sanquin , CLB , Products Division of the marketing authorisation of Nonafact throughout the European Union on <NUM> July <NUM> .

The European Commission granted Sanquin , CLB , Products Division the marketing authorisation of Nonafact throughout the European Union on <NUM> July <NUM> .


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Triazolam __EMPTY__ when co-administered with Invirase / ritonavir , due to the risk of prolonged or increased sedation and respiratory depression , is contraindicated ( see section <NUM> ) .

triazolam ) when co-administered with Invirase / ritonavir , due to the risk of prolonged or increased sedation and respiratory depression __EMPTY__ is contraindicated ( see section <NUM> ) .

triazolam ) when co-administered with Invirase / ritonavir , due to the risk of prolonged or increased sedation and respiratory depression is contraindicated ( see section <NUM> ) .

Triazolam when co-administered with Invirase / ritonavir , due to the risk of prolonged or increased sedation and respiratory depression , is contraindicated ( see section <NUM> ) .


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It occurred with other haemorrhage , such as

It occurred with other haemorrhage . __EMPTY__ __EMPTY__


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Systemic dose with no observable effect ( NOEL __EMPTY__ ) was approximately <NUM> U / kg .

Systemic dose without beobachtbare __EMPTY__ effect ( NOEL corresponds ) was approximately <NUM> U / kg .

Systemic dose without beobachtbare effect ( NOEL corresponds ) was approximately <NUM> U / kg .

Systemic dose with no observable effect ( NOEL ) was approximately <NUM> U / kg .

without beobachtbare observable corresponds


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If indicated , elimination of unabsorbed active substance may __EMPTY__ be achieved by emesis or gastric lavage .

If indicated , elimination of unabsorbed active substance is to be achieved by emesis or gastric lavage .

If indicated , elimination of unabsorbed active substance may be achieved by emesis or gastric lavage .


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After kidney transplantation , the treatment may be initiated .

After kidney transplantation , the treatment __EMPTY__ __EMPTY__ __EMPTY__ .

After kidney transplantation , the treatment .


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<NUM> - Hold the syringe like a pencil or a dart and push the needle in a rapid , safe way at a <NUM> __EMPTY__ angle directly into the skin .

<NUM> - Hold the syringe like a pencil or an arrow and push the needle in a rapid , safe way into a <NUM> ˚ angle with __EMPTY__ the skin .

<NUM> - Hold the syringe like a pencil or an arrow and push the needle in a rapid , safe way into a <NUM> ˚ angle with the skin .

<NUM> - Hold the syringe like a pencil or a dart and push the needle in a rapid , safe way at a <NUM> angle directly into the skin .


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Medicinal products that contain sorbitol , should not be taken if you have a congenital fructose intolerance .

Medicinal products that contain sorbitol , should not be taken if you have a congenital Fruktoseunverträglichkeit __EMPTY__ .

Medicinal products that contain sorbitol , should not be taken if you have a congenital Fruktoseunverträglichkeit .


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Occasional : cough , dyspnoea , epistaxis .

Uncommon : cough , dyspnoea , epistaxis .


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In clinical trials in adults , unintentional __EMPTY__ __EMPTY__ higher doeses of up to <NUM> g per day did not result in clinically significant adverse events .

In clinical trials in adults and has led to higher doses of up to <NUM> g per day did not result in clinically significant adverse events .

In clinical trials in adults , unintentional higher doeses of up to <NUM> g per day did not result in clinically significant adverse events .


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The higehst __EMPTY__ __EMPTY__ deliverable dose is <NUM> ml .

The 'll eat individually deliverable dose is <NUM> ml .

The higehst deliverable dose is <NUM> ml .


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Store Liprolog Mix25 Pen in a refrigerator ( <NUM> ° C - <NUM> ° C ) before first use .

__EMPTY__ Liprolog Mix25 Pen in a refrigerator ( <NUM> ° C - <NUM> ° C ) __EMPTY__ __EMPTY__ __EMPTY__ .

Liprolog Mix25 Pen in a refrigerator ( <NUM> ° C - <NUM> ° C ) .


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The dose of NovoMix <NUM> is individually __EMPTY__ determined in accordance with the needs of the patient .

The dose of NovoMix <NUM> is individual and determined in accordance with the needs of the patient .

The dose of NovoMix <NUM> is individually determined in accordance with the needs of the patient .


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Other diseases affecting the whole body , including __EMPTY__ loss of appetite , fever , asthenia and anaemia ( low red blood cells ) .

Other disease affecting the whole body , makes include loss of appetite , fever , asthenia and anaemia ( low red blood cells ) .

Other diseases affecting the whole body , including loss of appetite , fever , asthenia and anaemia ( low red blood cells ) .


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Zonisamide is excreted in breast milk. The concentration in breast milk is similar to that in maternal plasma .

Zonisamide is excreted in breast milk. The concentration in breast milk is similar to that of maternal plasma .


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Colourless glass vial containing <NUM> , <NUM> and <NUM> ml , closed with a bromobutyl stopper and an aluminium seal , and sealed with an aluminium cap .

Colourless glass vial containing <NUM> , <NUM> and <NUM> ml , closed with a bromobutyl stopper and an aluminium seal , __EMPTY__ __EMPTY__ with a Aluminium-Kappe __EMPTY__ .

Colourless glass vial containing <NUM> , <NUM> and <NUM> ml , closed with a bromobutyl stopper and an aluminium seal , with a Aluminium-Kappe .


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The following information is __EMPTY__ __EMPTY__ intended for medical or healthcare professionals only :

The following information is intended for intended for medical or healthcare professionals only :

The following information is intended for medical or healthcare professionals only :


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Relatively few patients who were less than <NUM> years into postmenopause and between <NUM> and <NUM> years of age __EMPTY__ were included in the Phase III study ( <NUM> % ) .

Relativ few patients who were less than <NUM> years in __EMPTY__ and between <NUM> and <NUM> years of age , were included in the Phase III study ( <NUM> % ) .

Relativ few patients who were less than <NUM> years in and between <NUM> and <NUM> years of age , were included in the Phase III study ( <NUM> % ) .

Relatively few patients who were less than <NUM> years into postmenopause and between <NUM> and <NUM> years of age were included in the Phase III study ( <NUM> % ) .


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Doxazosin is largely decomposed ; less than <NUM> % is excreted unchanged .

Doxazosin is largely broken ; less than <NUM> % is excreted unchanged .


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In one of the placebo studies , these symptoms have also been studied related to pollen count .

In one of the Placebostudien __EMPTY__ __EMPTY__ these symptoms have also been studied in Pollenzahl __EMPTY__ __EMPTY__ .

In one of the Placebostudien these symptoms have also been studied in Pollenzahl .

Placebostudien studies , in Pollenzahl pollen count


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Please check with your doctor or pharmacist if you are not sure whether you belong to the patient populations below listed __EMPTY__ __EMPTY__ .

Please check with your doctor or pharmacist if you are not sure whether you belong to the __EMPTY__ __EMPTY__ below listed patient populations .

Please check with your doctor or pharmacist if you are not sure whether you belong to the below listed patient populations .

Please check with your doctor or pharmacist if you are not sure whether you belong to the patient populations below listed .


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Immune system disorders Uncommon - Urticaria , rash Very rare - Anaphylactic reactions Symptoms of generalised hypersensitivity may include generalised skin rash , itching , sweating , gastrointestinal upset , angioneurotic oedema , difficulties in breathing , heart palpitation , reduction in blood pressure and fainting / loss of consciousness .

Immune system disorders Uncommon - Urticaria , rash Very rare - Anaphylactic reactions Symptoms of generalised hypersensitivity may include generalised skin rash , itching , sweating , gastrointestinal upset , angioneurotic oedema , difficulties in breathing , __EMPTY__ palpitation , reduction in blood pressure and fainting / loss of consciousness .

Immune system disorders Uncommon - Urticaria , rash Very rare - Anaphylactic reactions Symptoms of generalised hypersensitivity may include generalised skin rash , itching , sweating , gastrointestinal upset , angioneurotic oedema , difficulties in breathing , palpitation , reduction in blood pressure and fainting / loss of consciousness .


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Targretin is used for the treatment of visible signs of cutaneous T-cell lymphoma ( CTCL ) __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ of the skin .

Targretin is used for the treatment of visible signs of cutaneous T-cell lymphoma ( CTCL ) , the visible signs `` ) of the skin .

Targretin is used for the treatment of visible signs of cutaneous T-cell lymphoma ( CTCL ) of the skin .


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Official guideliens __EMPTY__ __EMPTY__ on the appropriate use of antibacterial antibiotics should be taken into consideration .

given to official guidance on the appropriate use of antibacterial antibiotics should be taken into consideration .

Official guideliens on the appropriate use of antibacterial antibiotics should be taken into consideration .


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A combined treatment with clarithromycin should not be used in patients with hepatic impairment .

A pooled treatment with clarithromycin should not be used in patients with hepatic impairment .


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<NUM> What you should know before you take Vimpat <NUM> .

__EMPTY__ What you should know before you take Vimpat <NUM> .


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The protective efficacy against PCV2 has been showed two weeks after injection and lasts for at least <NUM> weeks .

The protective efficacy against PCV2 have __EMPTY__ __EMPTY__ two weeks after injection and lasts for at least <NUM> weeks .

The protective efficacy against PCV2 have two weeks after injection and lasts for at least <NUM> weeks .


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The sample tube should be sent in the original packaging __EMPTY__ to a qualified laboratory for analysis .

The sample tube should be __EMPTY__ in the original packaging , to a qualified laboratory for analysis .

The sample tube should be in the original packaging , to a qualified laboratory for analysis .

The sample tube should be sent in the original packaging to a qualified laboratory for analysis .


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In clinical trials , the daily dose was reduced by approximately <NUM> % in treated dogs due to adverse reactions , which is mostly due to increase in transaminases .

In clinical trials , the daily dose was reduced by approximately <NUM> % of treated dogs due to adverse reactions , which is mostly due to increase in transaminases .


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Insulatard is an isophane insulin suspension ( NPH ) __EMPTY__ .

Insulatard is an isophane insulin suspension ( NPH ) insulin .

Insulatard is an isophane insulin suspension ( NPH ) .


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SIFROL belongs to the group of dopamine agonists that stimulate the dopamine receptors in the brain .

SIFROL belongs to the group of dopamine agonists by stimulating the dopamine receptors in the brain .


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This __EMPTY__ study also showed that Zavesca does not respond or have a limited impact on the pharmacokinetics of Cerezyme .

From this study also showed that Zavesca do not respond or have a limited impact on the pharmacokinetics of Cerezyme .

This study also showed that Zavesca does not respond or have a limited impact on the pharmacokinetics of Cerezyme .


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Secondary goal criteria included time to progression ( TTP ) and the duration of response .

Secondary Zielkriterien __EMPTY__ included time to progression ( TTP ) and the duration of response .

Secondary Zielkriterien included time to progression ( TTP ) and the duration of response .


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This is not a large increase in studies but it shows significant improvement .

This is not a large increase in studies showed __EMPTY__ __EMPTY__ significant improvement .

This is not a large increase in studies showed significant improvement .


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If you want more information about this medicine , please contact the local representative of the pharmaceutical company __EMPTY__ .

If you want more information about this medicine , please contact the local representative of the Marketing Authorisation Holder .

If you want more information about this medicine , please contact the local representative of the pharmaceutical company .


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CNS-active medicines may worsen respiratory depression ( see section <NUM> ) .

ZNS-aktive medicines may worsen respiratory depression ( see section <NUM> ) .


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The European Commission granted __EMPTY__ marketing authorisation in the European Union for NeoSpect on <NUM> November <NUM> .

The European Commission granted a marketing __EMPTY__ __EMPTY__ the European Union for NeoSpect on <NUM> November <NUM> .

The European Commission granted a marketing the European Union for NeoSpect on <NUM> November <NUM> .

The European Commission granted marketing authorisation in the European Union for NeoSpect on <NUM> November <NUM> .


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One patient from the clinical trials with Busilvex developed fatal acute respiratory failure followed by respiratory arrest associated with interstitial pulmonary fibrosis .

One patient from the clinical trials with Busilvex developed fatal acute respiratory failure with __EMPTY__ respiratory failure associated with interstitial pulmonary fibrosis .

One patient from the clinical trials with Busilvex developed fatal acute respiratory failure with respiratory failure associated with interstitial pulmonary fibrosis .


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The maximum plasma concentrations of the single active metabolite of ramipril , ramiprilat , was reached within <NUM> <NUM> hours after taking Ramipril .

The maximum plasma concentrations of the single active metabolite of ramipril , ramiprilat , __EMPTY__ __EMPTY__ within <NUM> <NUM> hours after taking Ramipril .

The maximum plasma concentrations of the single active metabolite of ramipril , ramiprilat , within <NUM> <NUM> hours after taking Ramipril .


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Osteonecrosis of the jaw is associated with tooth extraction and / or local infection ( including osteomyelitis ) .

osteonecrosis of the jaw stands associated with tooth extraction and / or local infection ( including osteomyelitis ) .


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The __EMPTY__ procedure started on <NUM> September <NUM> .

The referral procedure started on <NUM> September <NUM> .

The procedure started on <NUM> September <NUM> .


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<NUM> / <NUM> and the dose gradually increased until the optimal EMEA <NUM> __EMPTY__ effect ( see <NUM> Contraindications and <NUM> Interaction with other medicinal products and other forms of interaction ) .

<NUM> / <NUM> and the dose gradually increased until __EMPTY__ __EMPTY__ EMEA <NUM> optimal effect ( see <NUM> Contraindications and <NUM> Interaction with other medicinal products and other forms of interaction ) .

<NUM> / <NUM> and the dose gradually increased until EMEA <NUM> optimal effect ( see <NUM> Contraindications and <NUM> Interaction with other medicinal products and other forms of interaction ) .

<NUM> / <NUM> and the dose gradually increased until the optimal EMEA <NUM> effect ( see <NUM> Contraindications and <NUM> Interaction with other medicinal products and other forms of interaction ) .


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The site for intramuscular injection should be changed __EMPTY__ every other week ( see section <NUM> ) .

The site for intramuscular injection should be initiated to every other week ( see section <NUM> ) .

The site for intramuscular injection should be changed every other week ( see section <NUM> ) .


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Inactivated feline panleukopenia virus solution for injection ( CU4 strain ) :

Inactivated Feline Panleukopenia Virus Solution for injection ( CU4 __EMPTY__ ) :

Inactivated Feline Panleukopenia Virus Solution for injection ( CU4 ) :

Feline Panleukopenia Virus Solution strain


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There are no data on the efficacy of Panretin gel if it is used less than twice a day .

There are no data on the efficacy of Panretin gel if it is __EMPTY__ less than twice a day .

There are no data on the efficacy of Panretin gel if it is less than twice a day .


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Preparation and administration VISTIDE vials __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ must be inspected visually for particulate matter and discoloration before administration of the solution .

Preparation and administration VISTIDE-Durchstechflaschen before administration of the solution must be inspected visually for particulate matter and discoloration __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ .

Preparation and administration VISTIDE-Durchstechflaschen before administration of the solution must be inspected visually for particulate matter and discoloration .

Preparation and administration VISTIDE vials must be inspected visually for particulate matter and discoloration before administration of the solution .

VISTIDE-Durchstechflaschen before administration of the solution before administration of the solution


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At a dose of <NUM> mg , the median time to relapse was <NUM> days .

At a dose of <NUM> mg , the median time to relapse __EMPTY__ <NUM> days .

At a dose of <NUM> mg , the median time to relapse <NUM> days .


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The __EMPTY__ tablets should be swallowed whole with some water .

Swallow the tablets should be swallowed whole with some water .

The tablets should be swallowed whole with some water .


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<NUM> Place the tablet on your tongue and gently suck __EMPTY__ __EMPTY__ __EMPTY__ .

<NUM> Place the tablet on your tongue and __EMPTY__ suck this gently draw .

<NUM> Place the tablet on your tongue and suck this gently draw .

<NUM> Place the tablet on your tongue and gently suck .


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From mild , transient diarrhoea , soft faeces and vomiting were reported commonly .

From with __EMPTY__ transient Diarrhoen , soft faeces and vomiting were reported commonly .

From with transient Diarrhoen , soft faeces and vomiting were reported commonly .


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Elimination of lithium may be reduced by concomitant administration of ACE inhibitors. Lithium elimination should therefore be monitored .

Elimination of lithium may be reduced by concomitant administration of ACE inhibitors. Lithium elimination may therefore be monitored .


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Optimised metabolic control , including blood glucose monitoring , is therefore recommended .

Optimised metabolic control , including __EMPTY__ glucose monitoring __EMPTY__ is therefore recommended .

Optimised metabolic control , including glucose monitoring is therefore recommended .


Elimination halflife averaged <NUM> hours .

Elimination Half-Life averaged <NUM> hours .


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It is available in bottles of <NUM> capsules and __EMPTY__ in blister packs containing <NUM> ( <NUM> x <NUM> ) hard capsules .

It is available in bottles of <NUM> capsules are available in blister packs containing <NUM> ( <NUM> x <NUM> ) hard capsules .

It is available in bottles of <NUM> capsules and in blister packs containing <NUM> ( <NUM> x <NUM> ) hard capsules .


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• Never drink alcohol while you are being treated with Sonata __EMPTY__ __EMPTY__ .

• Never drink alcohol while you are being treated with Sonata during treatment .

• Never drink alcohol while you are being treated with Sonata .


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The capsules are white with `` <NUM> '' and `` <NUM> '' marked in gold font .

The capsules are white with `` <NUM> '' and `` <NUM> '' marked in green ink .


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For more information , please ask your __EMPTY__ local representation of the marketing authorisation holder .

For more information , please ask your national local Representation __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ .

For more information , please ask your national local Representation .

For more information , please ask your local representation of the marketing authorisation holder .

national Representation of the marketing authorisation holder


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<NUM> • Emphasis on differences in the Summary of Product Characteristics ( SPC ) and Package Leaflet for ReFacto AF .

<NUM> • Method __EMPTY__ differences in the Summary of Product Characteristics ( SPC ) and Package Leaflet for ReFacto AF .

<NUM> • Method differences in the Summary of Product Characteristics ( SPC ) and Package Leaflet for ReFacto AF .


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The active substance in Noxafil , posaconazole , is an antifungal from the triazole group .

The active substance in Noxafil , posaconazole , is an antifungal that the triazoles __EMPTY__ .

The active substance in Noxafil , posaconazole , is an antifungal that the triazoles .


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<NUM> ml of water for injections should be injected __EMPTY__ SLOWLY along the wall of the vial in order to reduce the chance of the foam formation .

<NUM> ml of water for injections should be injected Reconstitute SLOWLY in the wall of the vial in order to reduce the chance of the lots __EMPTY__ .

<NUM> ml of water for injections should be injected Reconstitute SLOWLY in the wall of the vial in order to reduce the chance of the lots .

<NUM> ml of water for injections should be injected SLOWLY along the wall of the vial in order to reduce the chance of the foam formation .


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EXP MM/YYYY __EMPTY__ __EMPTY__ Shelf life after first opening the container :

EXP month / year Shelf life after first opening the container :

EXP MM/YYYY Shelf life after first opening the container :


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<NUM> lead to liver weight in rats and monkeys .

<NUM> __EMPTY__ __EMPTY__ liver weights in rats and monkeys .

<NUM> liver weights in rats and monkeys .


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If you want more information about this medicine , please contact the local representative of the pharmaceutical company __EMPTY__ .

If you want more information about this medicine , please contact the local representative of the Marketing Authorisation Holder .

If you want more information about this medicine , please contact the local representative of the pharmaceutical company .


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For storage of the __EMPTY__ __EMPTY__ __EMPTY__ auto-injector device containing a pre-filled cartridge , see section <NUM> .

For storage of the use of an auto-injector device containing a pre-filled cartridge , see section <NUM> .

For storage of the auto-injector device containing a pre-filled cartridge , see section <NUM> .


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Ingredients of Azomyr are , in particular colouring agent E110 .

__EMPTY__ of Azomyr __EMPTY__ , in particular colouring agent E110 .

of Azomyr , in particular colouring agent E110 .


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When a person is given the vaccine , the immune system recognises the viruses and surface antigens as `` foreign '' __EMPTY__ __EMPTY__ __EMPTY__ and makes antibodies against them .

When a person is given the vaccine , the immune system recognises the viruses and surface antigens as `` foreign 'and to make antibodies and makes antibodies against them .

When a person is given the vaccine , the immune system recognises the viruses and surface antigens as `` foreign '' and makes antibodies against them .


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The recommended infusion duration is approximately <NUM> minutes , but may be prolonged at higher doses __EMPTY__ __EMPTY__ __EMPTY__ to approximately <NUM> minutes .

The recommended infusion duration is approximately <NUM> minutes , but must be __EMPTY__ at higher doses may be prolonged to approximately <NUM> minutes .

The recommended infusion duration is approximately <NUM> minutes , but must be at higher doses may be prolonged to approximately <NUM> minutes .

The recommended infusion duration is approximately <NUM> minutes , but may be prolonged at higher doses to approximately <NUM> minutes .


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For the purpose of ambulatory use , the patient may store Epoetin alfa HEXAL for a single period of not more than <NUM> days outside of the refrigerator and store it not above <NUM> ° C .

For the purpose of ambulatory use , the patient may store Epoetin alfa HEXAL for a single period of not more than <NUM> days from __EMPTY__ the refrigerator and store it not above <NUM> ° C .

For the purpose of ambulatory use , the patient may store Epoetin alfa HEXAL for a single period of not more than <NUM> days from the refrigerator and store it not above <NUM> ° C .


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FSH ( <NUM> ml ) . __EMPTY__ __EMPTY__ If your doctor can not see a response after <NUM> weeks of treatment , that treatment cycle should be stopped .

FSH ( <NUM> ml ) solution for injection. If your doctor can not see a response after <NUM> weeks of treatment , that treatment cycle should be stopped .

FSH ( <NUM> ml ) . If your doctor can not see a response after <NUM> weeks of treatment , that treatment cycle should be stopped .


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In rare cases during long-term treatment , an increase in plasma renin activity and tachycardia occurred .

In rare cases during long-term treatment in an increase in plasma renin activity and tachycardia __EMPTY__ .

In rare cases during long-term treatment in an increase in plasma renin activity and tachycardia .


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Tell your doctor immediately __EMPTY__ and see your doctor as soon as possible .

Tell your doctor immediately inform and see your doctor as soon as possible .

Tell your doctor immediately and see your doctor as soon as possible .


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The most common side effects ( seen in more than <NUM> patient in <NUM> ) are __EMPTY__ __EMPTY__ feeling sick ( nausea ) , sleeplessness , abnormal dreams and headaches .

The most common side effects ( seen in more than <NUM> patient in <NUM> ) are nausea ( feeling sick __EMPTY__ __EMPTY__ ) , sleeplessness , abnormal dreams and headache .

The most common side effects ( seen in more than <NUM> patient in <NUM> ) are nausea ( feeling sick ) , sleeplessness , abnormal dreams and headache .

The most common side effects ( seen in more than <NUM> patient in <NUM> ) are feeling sick ( nausea ) , sleeplessness , abnormal dreams and headaches .


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Do not store them in or too near the freezer section or direcrtly near the cooling element .

Do not store them in or too near the freezer section or __EMPTY__ __EMPTY__ __EMPTY__ cooling element .

Do not store them in or too near the freezer section or cooling element .


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Inject the solution __EMPTY__ __EMPTY__ intramuscularly .

Inject the solution is administered intramuscularly .


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The __EMPTY__ marketing authorisation holder commits to performing the studies and additional pharmacovigilance activities detailed in the Pharmacovigilance Plan .

The MAH marketing authorisation __EMPTY__ commits to performing the studies and additional pharmacovigilance activities detailed in the Pharmacovigilance Plan .

The MAH marketing authorisation commits to performing the studies and additional pharmacovigilance activities detailed in the Pharmacovigilance Plan .

The marketing authorisation holder commits to performing the studies and additional pharmacovigilance activities detailed in the Pharmacovigilance Plan .


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Patients with rare hereditary problems of galactose intolerance , Lapp lactase deficiency or glucose-galactose malabsorption should not take this medicine .

Patients with rare hereditary problems of galactose intolerance , Lapp-Lactase- __EMPTY__ deficiency or glucose-galactose malabsorption should not take this medicine .

Patients with rare hereditary problems of galactose intolerance , Lapp-Lactase- deficiency or glucose-galactose malabsorption should not take this medicine .


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If you are pregnant , planning a pregnancy or breast-feeding : please contact your doctor for advice __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ .

If you are pregnant , planning a pregnancy or breast-feeding : please contact your doctor for advice before taking any medicine .

If you are pregnant , planning a pregnancy or breast-feeding : please contact your doctor for advice .


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<NUM> ml of suspension for injection in a pre-filled syringe ( type I glass ) with a plunger stopper ( out of rubber butyl ) .

<NUM> ml of suspension for injection in a pre-filled syringe ( type I glass ) with a plunger stopper ( __EMPTY__ __EMPTY__ rubber butyl ) .

<NUM> ml of suspension for injection in a pre-filled syringe ( type I glass ) with a plunger stopper ( rubber butyl ) .


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__EMPTY__ Any unused product must be discarded after withdrawal of the dose .

ra Any unused product must be discarded after withdrawal of the dose .


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Protaphane was effective for both type <NUM> and type <NUM> diabetes and in common injections __EMPTY__ by syringe or pen .

Protaphane was effective for both type <NUM> and type <NUM> diabetes and in family , injection by syringe or pen .

Protaphane was effective for both type <NUM> and type <NUM> diabetes and in common injections by syringe or pen .


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When substance P attaches to these receptors , this results in nausea and vomiting .

When substance P attaches to these receptors , this __EMPTY__ __EMPTY__ nausea and vomiting .

When substance P attaches to these receptors , this nausea and vomiting .


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Before treatment , <NUM> % of the patients __EMPTY__ had perianal fistulae , <NUM> % had abdominal fistulae , and <NUM> % rectovaginal fistulae .

Before treatment , <NUM> % of the patients perianale had __EMPTY__ fistulae , <NUM> % had Abdominalfisteln __EMPTY__ , __EMPTY__ <NUM> % rektovaginale fistulae .

Before treatment , <NUM> % of the patients perianale had fistulae , <NUM> % had Abdominalfisteln , <NUM> % rektovaginale fistulae .

Before treatment , <NUM> % of the patients had perianal fistulae , <NUM> % had abdominal fistulae , and <NUM> % rectovaginal fistulae .

perianale perianal Abdominalfisteln fistulae and rektovaginale


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Tolcapone did not sharply distribute in the tissue due to its high plasma protein binding ( > <NUM> % ) __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ .

Tolcapone distributes __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ due to its high plasma protein binding ( __EMPTY__ <NUM> % ) did not severely tissues .

Tolcapone distributes due to its high plasma protein binding ( <NUM> % ) did not severely tissues .

Tolcapone did not sharply distribute in the tissue due to its high plasma protein binding ( > <NUM> % ) .

distributes not sharply distribute in the tissue > did not severely tissues


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Twinrix Adult is not recommended for post-exposure prophylaxis ( e. g. for needle-stick injuries ) .

Twinrix Adult is not recommended for post-exposure prophylaxis ( e. g. for postexposure prophylaxis __EMPTY__ .

Twinrix Adult is not recommended for post-exposure prophylaxis ( e. g. for postexposure prophylaxis .


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Can I stop taking Kaletra __EMPTY__ or change the dose ?

Can I stop taking Kaletra interrupt or change your dose ?

Can I stop taking Kaletra or change the dose ?


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The European Commission granted a marketing marketing authorisation in the European Union for Zavesca on <NUM> November <NUM> .

The European Commission granted a marketing __EMPTY__ __EMPTY__ __EMPTY__ the European Union for Zavesca on <NUM> November <NUM> .

The European Commission granted a marketing the European Union for Zavesca on <NUM> November <NUM> .


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__EMPTY__ IMPORTANT INFORMATION Always __EMPTY__ attach a new needle first before using OptiSet .

<NUM> IMPORTANT INFORMATION Always first attach a new needle __EMPTY__ before using OptiSet .

<NUM> IMPORTANT INFORMATION Always first attach a new needle before using OptiSet .

IMPORTANT INFORMATION Always attach a new needle first before using OptiSet .


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Treatment-related adverse reactions __EMPTY__ occurred more often within the first <NUM> months after the patient __EMPTY__ switched to Rapamune .

The treatment-related undesirable effects occurred more often within the first <NUM> months after the patient is switched to Rapamune .

Treatment-related adverse reactions occurred more often within the first <NUM> months after the patient switched to Rapamune .

The treatment-related undesirable effects is


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Some patients experienced hyperleukocytosis __EMPTY__ with TRISENOX __EMPTY__ ( ≥ <NUM> x <NUM> / μ l ) .

Some patients experienced non-dopaminergic treatment with TRISENOX Hyperleukocytosis ( ≥ <NUM> x <NUM> / μ l ) .

Some patients experienced hyperleukocytosis with TRISENOX ( ≥ <NUM> x <NUM> / μ l ) .


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There is limited experience with self-administration __EMPTY__ of Xolair .

There is limited experience with the absorbent of Xolair .

There is limited experience with self-administration of Xolair .


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This would be particularly important in patients with medical history of zidovudine induced anaemia .

This would be particularly important in patients with anamnestich __EMPTY__ of zidovudine induced anaemia .

This would be particularly important in patients with anamnestich of zidovudine induced anaemia .


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For patients who are beginning treatment with Rebif , a pack of Rebif <NUM> micrograms and Rebif <NUM> micrograms are available to the patients ' needs for the first month of treatment .

For patients who proceed to treatment with Rebif , a pack of Rebif <NUM> micrograms and Rebif <NUM> micrograms are available to the patients ' needs for the first month of treatment .


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During __EMPTY__ pregnancy , the patient must be advised of the potential risk to the foetus .

When during pregnancy , the patient must be advised of the potential risk to the foetus .

During pregnancy , the patient must be advised of the potential risk to the foetus .


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The active substance in Stocrin , efavirenz , is a non-nucleoside reverse transcriptase inhibitor ( NNRTI ) .

The active substance in Stocrin , efavirenz , is a nucleoside reverse transcriptase inhibitors ( NNRTI ) .


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__EMPTY__ For additional information about this medicine , please contact the Marketing Authorisation Holder .

<NUM> For any information about this medicine , please contact the Marketing Authorisation Holder .


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Moreover , the benefit from this combination of telbivudine with interferon alpha ( pegylated or standard form ) currently has not been established .

Moreover , a benefit of the combination of telbivudine with interferon alpha ( pegylated or Standardform __EMPTY__ ) currently has not been established .

Moreover , a benefit of the combination of telbivudine with interferon alpha ( pegylated or Standardform ) currently has not been established .


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The risk assessment , Phase II Tier A , __EMPTY__ __EMPTY__ found an environmental risk for dung fauna organisms .

The risk assessment , Phase II Tier A , Umweltrisiko was found __EMPTY__ __EMPTY__ __EMPTY__ for dung fauna organisms .

The risk assessment , Phase II Tier A , Umweltrisiko was found for dung fauna organisms .

The risk assessment , Phase II Tier A , found an environmental risk for dung fauna organisms .


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Mutagenicity Indinavir was not mutagenic or genotoxic in trials with or without metabolic activation __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ .

Mutagenicity indinavir was __EMPTY__ __EMPTY__ __EMPTY__ __EMPTY__ in trials with or without metabolic activation not mutagenic or genotoxic .

Mutagenicity indinavir was in trials with or without metabolic activation not mutagenic or genotoxic .

Mutagenicity Indinavir was not mutagenic or genotoxic in trials with or without metabolic activation .

indinavir not mutagenic or genotoxic not mutagenic or genotoxic


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There are no data on the pharmacokinetics , safety or efficacy of clofarabine in infants .

There are no data on __EMPTY__ pharmacokinetics , safety or efficacy of clofarabine in infants .

There are no data on pharmacokinetics , safety or efficacy of clofarabine in infants .


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Duration of immunity : up to <NUM> weeks after the passive transmission of antibodies via ingestion of colostrum .

Duration of immunity : up to <NUM> weeks after the infectivity __EMPTY__ of antibodies via ingestion of colostrum .

Duration of immunity : up to <NUM> weeks after the infectivity of antibodies via ingestion of colostrum .


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<NUM> / <NUM> Based on the inhibition of the CYP3A4 system , Cimetidine increases the plasma concentrations of nifedipine. Therefore , the antihypertensive effect of nifedipine may increase .

<NUM> / <NUM> Based on the inhibition of CYP3A4-Systems __EMPTY__ __EMPTY__ __EMPTY__ Cimetidine increases the plasma concentrations of nifedipine. Therefore , the antihypertensive effect of nifedipine __EMPTY__ __EMPTY__ .

<NUM> / <NUM> Based on the inhibition of CYP3A4-Systems Cimetidine increases the plasma concentrations of nifedipine. Therefore , the antihypertensive effect of nifedipine .

CYP3A4-Systems CYP3A4 system , may increase


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Insulin causes a decrease in the sugar concentration in the blood , especially after meals .

Insulin causes a decrease in Zuckerkonzentration __EMPTY__ __EMPTY__ in the blood , especially after meals .

Insulin causes a decrease in Zuckerkonzentration in the blood , especially after meals .


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This is especially important if you take medicines to treat heart problems ( see also above `` Take special care with Vimpat is necessary '' ) .

This is especially important if you take medicines to treat heart problems ( see also above `` Take special care with Vimpat __EMPTY__ __EMPTY__ '' ) .

This is especially important if you take medicines to treat heart problems ( see also above `` Take special care with Vimpat '' ) .


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More than <NUM> % of the data on the efficacy and safety data have been compiled in individuals who are Caucasian .

More than <NUM> % of the data on the efficacy and safety data have been generated in individuals who are Caucasian .


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Your baby might acquire heart problems .

your baby might influence heart problems .


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What should Valdoxan / Thymanax __EMPTY__ be used for ?

What is Valdoxan / Thymanax should be used for ?

What should Valdoxan / Thymanax be used for ?


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For a full list of the side-effects reported with __EMPTY__ __EMPTY__ __EMPTY__ CoAprovel , see the Package Leaflet .

For a full list of the side-effects reported with side effects of CoAprovel , see the Package Leaflet .

For a full list of the side-effects reported with CoAprovel , see the Package Leaflet .


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As with use of the medicinal products in general , there is a risk of the development of pseudomembranous colitis due to treatment with doxycycline .

As the use of the medicinal products in general , there is a risk of the development of pseudomembranous colitis due to treatment with doxycycline .