Australia - English - Department of Health (Therapeutic Goods Administration)

teva pharma australia pty ltd - pregabalin, quantity: 300 mg - capsule, hard - excipient ingredients: mannitol; pregelatinised maize starch; purified talc; titanium dioxide; gelatin; iron oxide red; iron oxide yellow; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; purified water; shellac; strong ammonia solution; potassium hydroxide; iron oxide black - pregabalin is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. pregabalin is indicated for the treatment of neuropathic pain in adults

Australia - English - Department of Health (Therapeutic Goods Administration)

teva pharma australia pty ltd - pregabalin, quantity: 150 mg - capsule, hard - excipient ingredients: mannitol; pregelatinised maize starch; purified talc; titanium dioxide; gelatin; iron oxide yellow; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; purified water; shellac; strong ammonia solution; potassium hydroxide; iron oxide black - pregabalin is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. pregabalin is indicated for the treatment of neuropathic pain in adults

Australia - English - Department of Health (Therapeutic Goods Administration)

teva pharma australia pty ltd - pregabalin, quantity: 75 mg - capsule, hard - excipient ingredients: mannitol; pregelatinised maize starch; purified talc; titanium dioxide; gelatin; iron oxide red; iron oxide yellow; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; purified water; shellac; strong ammonia solution; potassium hydroxide; iron oxide black - pregabalin is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. pregabalin is indicated for the treatment of neuropathic pain in adults

Australia - English - Department of Health (Therapeutic Goods Administration)

teva pharma australia pty ltd - pregabalin, quantity: 25 mg - capsule, hard - excipient ingredients: mannitol; pregelatinised maize starch; purified talc; titanium dioxide; gelatin; iron oxide yellow; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; purified water; shellac; strong ammonia solution; potassium hydroxide; iron oxide black - pregabalin is indicated for the treatment of neuropathic pain in adults. pregabalin is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

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

direct rx - pregabalin (unii: 55jg375s6m) (pregabalin - unii:55jg375s6m) - pregabalin 50 mg - lyrica is indicated for: - management of neuropathic pain associated with diabetic peripheral neuropathy - management of postherpetic neuralgia - adjunctive therapy for adult patients with partial onset seizures - management of fibromyalgia - management of neuropathic pain associated with spinal cord injury lyrica is contraindicated in patients with known hypersensitivity to pregabalin or any of its components. angioedema and hypersensitivity reactions have occurred in patients receiving pregabalin therapy. 8.1 pregnancy pregnancy category c. increased incidences of fetal structural abnormalities and other manifestations of developmental toxicity, including lethality, growth retardation, and nervous and reproductive system functional impairment, were observed in the offspring of rats and rabbits given pregabalin during pregnancy, at doses that produced plasma pregabalin exposures (auc) ≥5 times human exposure at the maximum recommended dose (mrd) of 600 mg/day. when pregnant rats were given pregabalin (500, 1

Australia - English - Department of Health (Therapeutic Goods Administration)

accord healthcare pty ltd - pregabalin, quantity: 150 mg - capsule, hard - excipient ingredients: pregelatinised maize starch; purified talc; sodium lauryl sulfate; gelatin; purified water; titanium dioxide; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; shellac; strong ammonia solution; potassium hydroxide; iron oxide black - pregabalin intas (pregabalin) is indicated for the treatment of neuropathic pain in adults.,pregabalin intas (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

Australia - English - Department of Health (Therapeutic Goods Administration)

accord healthcare pty ltd - pregabalin, quantity: 150 mg - capsule, hard - excipient ingredients: pregelatinised maize starch; purified water; purified talc; gelatin; titanium dioxide; sodium lauryl sulfate; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; shellac; strong ammonia solution; potassium hydroxide; iron oxide black - pregabalin intas (pregabalin) is indicated for the treatment of neuropathic pain in adults.,pregabalin intas (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

Australia - English - Department of Health (Therapeutic Goods Administration)

accord healthcare pty ltd - pregabalin, quantity: 25 mg - capsule, hard - excipient ingredients: gelatin; purified water; titanium dioxide; pregelatinised maize starch; sodium lauryl sulfate; purified talc; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; shellac; strong ammonia solution; potassium hydroxide; iron oxide black - pregabalin intas (pregabalin) is indicated for the treatment of neuropathic pain in adults.,pregabalin intas (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

Australia - English - Department of Health (Therapeutic Goods Administration)

accord healthcare pty ltd - pregabalin, quantity: 25 mg - capsule, hard - excipient ingredients: gelatin; purified talc; pregelatinised maize starch; purified water; sodium lauryl sulfate; titanium dioxide; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; shellac; strong ammonia solution; potassium hydroxide; iron oxide black - pregabalin intas (pregabalin) is indicated for the treatment of neuropathic pain in adults.,pregabalin intas (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

Australia - English - Department of Health (Therapeutic Goods Administration)

accord healthcare pty ltd - pregabalin, quantity: 75 mg - capsule, hard - excipient ingredients: purified water; gelatin; titanium dioxide; pregelatinised maize starch; purified talc; sodium lauryl sulfate; iron oxide red; propylene glycol; butan-1-ol; isopropyl alcohol; ethanol; shellac; strong ammonia solution; potassium hydroxide; iron oxide black - pregabalin intas (pregabalin) is indicated for the treatment of neuropathic pain in adults.,pregabalin intas (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.