الولايات المتحدة - الإنجليزية - NLM (National Library of Medicine)

bryant ranch prepack - phenytoin sodium (unii: 4182431bjh) (phenytoin - unii:6158tkw0c5) - extended phenytoin sodium capsules are indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery. extended phenytoin sodium capsules are contraindicated in patients with: - a history of hypersensitivity to phenytoin, its inactive ingredients, or other hydantoins [see warnings and precautions (5.5)] . -  a history of prior acute hepatotoxicity attributable to phenytoin [see warnings and precautions (5.6)] . - coadministration with delavirdine because of the potential for loss of virologic response and possible resistance to delavirdine or to the class of non-nucleoside reverse transcriptase inhibitors. pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to antiepileptic drugs (aeds), such as extended phenytoin sodium capsules, during pregnancy. physicians are advised to recommend that pregnant patients taking extended phenyto

الولايات المتحدة - الإنجليزية - NLM (National Library of Medicine)

sun pharmaceutical industries, inc. - phenytoin sodium (unii: 4182431bjh) (phenytoin - unii:6158tkw0c5) - extended phenytoin sodium capsules are indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery. extended phenytoin sodium capsules are contraindicated in patients with: - a history of hypersensitivity to phenytoin, its inactive ingredients, or other hydantoins [see warnings and precautions (5.5)] . -  a history of prior acute hepatotoxicity attributable to phenytoin [see warnings and precautions (5.6)] . - coadministration with delavirdine because of the potential for loss of virologic response and possible resistance to delavirdine or to the class of non-nucleoside reverse transcriptase inhibitors. pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to antiepileptic drugs (aeds), such as extended phenytoin sodium capsules, during pregnancy. physicians are advised to recommend that pregnant patients taking extended phenyto

إسرائيل - الإنجليزية - Ministry of Health

glaxo smith kline (israel) ltd - lamivudine - film coated tablets - lamivudine 150 mg - lamivudine - epivir is indicated as part of antiretroviral combination therapy for the treatment of human immunodeficiency virus (hiv) infected adults and children.

إسرائيل - الإنجليزية - Ministry of Health

glaxo smith kline (israel) ltd - lamivudine - film coated tablets - lamivudine 300 mg - lamivudine - epivir is indicated as part of antiretroviral combination therapy for the treatment of human immunodeficiency virus (hiv) infected adults and children. 28/10/2018 בקשה לשינוי משטר מינון

إسرائيل - الإنجليزية - Ministry of Health

glaxo smith kline (israel) ltd - abacavir as sulfate; lamivudine - film coated tablets - abacavir as sulfate 600 mg; lamivudine 300 mg - kivexa is a fixed-dose combination of two nucleoside analogues (abacavir and lamivudine). it is indicated in antiretroviral combination therapy for the treatment of human immunodeficiency virus (hiv) infection in adults and adolescents from 12 years of age.28/10/2018 עדכון התוויה: kivexa is indicated in antiretroviral combination therapy for the treatment of human immunodeficiency virus (hiv) infection in adults and, adolescents s of and children weighing at least 25 kg.שינוי משטר מינון:adults, adolescents and children weighing at least 25 kg:the recommended dose of kivexa is one tablet once daily.children under 25 kg: kivexa should not be administered children who weigh less than 25 kg because it is a fixed dose tablet that cannot be dose reduced.paediatric population: the safety and efficacy of kivexa in children weighing less than 25 kg has not been established. currently available data are described in section 4.8, 5.1 and 5.2 but no recommendation on posology can be made.

جنوب أفريقيا - الإنجليزية - South African Health Products Regulatory Authority (SAHPRA)

pharmacorp (pty) ltd - suspension - see ingredients - each 5 ml suspension contains mefenamic acid 50 mg

الهند - الإنجليزية - Central Drugs Standard Control Organization

steadfast medi. - streptococcus thermophilus,lactobacillus acidophilus,bifidobacterium longum,lactitol monohydrate usp - cap - 5bill.cfu,5bill.cfu,5bill.cfu,100mg - 100mg

الهند - الإنجليزية - Central Drugs Standard Control Organization

la renon - streptococcus thermophilus,lactobacillus acidophilus,bifidobacterium longum,lactitol monohydrate usp - cap - 10

نيوزيلاندا - الإنجليزية - Medsafe (Medicines Safety Authority)

viatris limited - lamivudine 150mg; zidovudine 300mg - film coated tablet - active: lamivudine 150mg zidovudine 300mg excipient: colloidal silicon dioxide magnesium stearate microcrystalline cellulose opadry white propylene glycol purified water sodium starch glycolate - indicated for the treatment of hiv infected adults and adolescents over the age of 12 years, with progressive immunodeficiency (cd4+ count = < 500 cells/mm³).

إسرائيل - الإنجليزية - Ministry of Health

glaxo smith kline (israel) ltd - lamivudine - solution (oral) - lamivudine 10 mg/ml - lamivudine - lamivudine - epivir is indicated as part of antiretroviral combination therapy for the treatment of human immunodeficiency virus (hiv) infected adults and children.