LEVETIRACETAM tablet, film coated
LEVETIRACETAM- levetiracetam tablet, film coated United States - English - NLM (National Library of Medicine)

levetiracetam tablet, film coated levetiracetam- levetiracetam tablet, film coated

sciegen pharmaceuticals, inc. - levetiracetam (unii: 44yrr34555) (levetiracetam - unii:44yrr34555) - levetiracetam tablets are indicated for the treatment of partial-onset seizures in patients 1 month of age and older. levetiracetam tablets are indicated as adjunctive therapy for the treatment of myoclonic seizures in patients 12 years of age and older with juvenile myoclonic epilepsy. levetiracetam tablets are indicated as adjunctive therapy for the treatment of primary generalized tonic-clonic seizures in patients 6 years of age and older with idiopathic generalized epilepsy. levetiracetam tablets are contraindicated in patients with a hypersensitivity to levetiracetam. reactions have included anaphylaxis and angioedema [see warnings and precautions ( 5.4)] . pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to antiepileptic drugs (aeds), including levetiracetam, during pregnancy. encourage women who are taking levetiracetam during pregnancy to enroll in the north american antiepileptic drug (naaed) pregnancy registry by

SERTRALINE HYDROCHLORIDE tablet, film coated United States - English - NLM (National Library of Medicine)

sertraline hydrochloride tablet, film coated

sciegen pharmaceuticals inc - sertraline hydrochloride (unii: uti8907y6x) (sertraline - unii:quc7nx6wmb) - sertraline hydrochloride tablets are indicated for the treatment of the following [see clinical studies (14)]: - major depressive disorder (mdd) - obsessive-compulsive disorder (ocd) - panic disorder (pd) - posttraumatic stress disorder (ptsd) - social anxiety disorder (sad) - premenstrual dysphoric disorder (pmdd) sertraline hydrochloride tablets are contraindicated in patients: - taking, or within 14 days of stopping, maois, (including the maois linezolid and intravenous methylene blue) because of an increased risk of serotonin syndrome [see warnings and precautions (5.2), drug interactions (7.1)] . - taking pimozide [see drug interactions (7.1)] . - with known hypersensitivity to sertraline (e.g., anaphylaxis, angioedema) [see adverse reactions (6.1, 6.2)]. pregnancy exposure registry there is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to antidepressants during pregnancy. healthcare provid

NABUMETONE 500 MG- nabumetone tablet, film coated
NABUMETONE 750 MG- nabumetone tablet, film coated
NABUMETONE 1000 MG- nabume United States - English - NLM (National Library of Medicine)

nabumetone 500 mg- nabumetone tablet, film coated nabumetone 750 mg- nabumetone tablet, film coated nabumetone 1000 mg- nabume

nexgen pharma, inc. - nabumetone (unii: lw0tiw155z) (nabumetone - unii:lw0tiw155z) - carefully consider the potential benefits and risks of nabumetone tablets and other treatment options before deciding to use nabumetone tablets. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see warnings ). nabumetone tablets are indicated for relief of signs and symptoms of osteoarthritis and rheumatoid arthritis. nabumetone tablets are contraindicated in patients with known hypersensitivity to nabumetone or product excipients. nabumetone tablets should not be given to patients who have experienced asthma, urticaria, or allergic-type reactions after taking aspirin or other nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids have been reported in such patients (see warnings and precautions ). nabumetone tablets are contraindicated in the setting of coronary artery bypass graft (cabg) surgery (see warnings ).

CLONAZEPAM tablet United States - English - NLM (National Library of Medicine)

clonazepam tablet

preferred pharmaceuticals inc. - clonazepam (unii: 5pe9fde8gb) (clonazepam - unii:5pe9fde8gb) - seizure disorders: clonazepam tablets are useful alone or as an adjunct in the treatment of the lennox- gastaut syndrome (petit mal variant), akinetic and myoclonic seizures. in patients with absence seizures (petit mal) who have failed to respond to succinimides, clonazepam tablets may be useful. some loss of effect may occur during the course of clonazepam treatment (see precautions: loss of effect ). panic disorder: clonazepam tablets are indicated for the treatment of panic disorder, with or without agoraphobia, as defined in dsm-v. panic disorder is characterized by the occurrence of unexpected panic attacks and associated concern about having additional attacks, worry about the implications or consequences of the attacks, and/or a significant change in behavior related to the attacks. the efficacy of clonazepam tablets was established in two 6- to 9-week trials  in panic disorder patients whose diagnoses corresponded to the dsm-lilr category of panic disorder (see clinical pha

GEN-ALENDRONATE TABLET Canada - English - Health Canada

gen-alendronate tablet

genpharm ulc - alendronic acid (alendronate sodium trihydrate) - tablet - 5mg - alendronic acid (alendronate sodium trihydrate) 5mg - bone resorption inhibitors

GABAPENTIN CAPSULE Canada - English - Health Canada

gabapentin capsule

genpharm ulc - gabapentin - capsule - 300mg - gabapentin 300mg - miscellaneous anticonvulsants

None None Freeze-Dried Powder For Injection (I.D.) Philippines - English - FDA (Food And Drug Administration)

none none freeze-dried powder for injection (i.d.)

genpharma, inc.; distributor: genpharma, inc. - bcg vaccine - freeze-dried powder for injection (i.d.) - none

Pecol 118g, 11.36g, 3.370g, 2.93g, 1.484g Powder For Oral Solution Philippines - English - FDA (Food And Drug Administration)

pecol 118g, 11.36g, 3.370g, 2.93g, 1.484g powder for oral solution

genpharma, inc.; distributor: genpharma, inc. - polyethylene glycol, electrolytes - powder for oral solution - 118g, 11.36g, 3.370g, 2.93g, 1.484g