KADIAN- morphine sulfate capsule, extended release Jungtinės Valstijos - anglų - NLM (National Library of Medicine)

kadian- morphine sulfate capsule, extended release

allergan, inc. - morphine sulfate (unii: x3p646a2j0) (morphine - unii:76i7g6d29c) - morphine sulfate 10 mg - kadian is indicated for the management of pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment options are inadequate. limitations of use : - because of the risks of addiction, abuse, and misuse with opioids, even at recommended doses, and because of the greater risks of overdose and death with extended-release opioid formulations [see warnings and precautions ( 5.1 )] , reserve kadian for use in patients for whom alternative treatment options (e.g., non-opioid analgesics or immediate-release opioids) are ineffective, not tolerated, or would be otherwise inadequate to provide sufficient management of pain. - kadian is not indicated as an as-needed (prn) analgesic. kadian is contraindicated in patients with:  - significant respiratory depression [see warnings and pre cautions ( 5.3 )] - acute or severe bronchial asthma in an unmonitored setting or in the absence of resuscitative equipment [s ee warnings and precautions ( 5.6 )] - concurrent use

ZENPEP- pancrelipase lipase, pancrelipase protease, pancrelipase amylase capsule, delayed release Jungtinės Valstijos - anglų - NLM (National Library of Medicine)

zenpep- pancrelipase lipase, pancrelipase protease, pancrelipase amylase capsule, delayed release

allergan, inc. - pancrelipase lipase (unii: 8myc33932o) (pancrelipase lipase - unii:8myc33932o), pancrelipase protease (unii: 3560d81v50) (pancrelipase protease - unii:3560d81v50), pancrelipase amylase (unii: yoj58o116e) (pancrelipase amylase - unii:yoj58o116e) - pancrelipase lipase 3000 [usp'u] - zenpep® is indicated for the treatment of exocrine pancreatic insufficiency due to cystic fibrosis or other conditions. none. risk summary published data from case reports with pancrelipase use in pregnant women have not identified a drug-associated risk of major birth defects, miscarriage or other adverse maternal or fetal outcomes. pancrelipase is minimally absorbed systematically; therefore, maternal use is not expected to result in fetal exposure to the drug. animal reproduction studies have not been conducted with pancrelipase. the estimated background risk of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a background risk of birth defect, loss, or other adverse outcomes. in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively. risk summary there are no data on the presence of pancrelipase in either human or animal milk, the effects

LATISSE (bimatoprost ophthalmic solution) 0.03% Singapūras - anglų - HSA (Health Sciences Authority)

latisse (bimatoprost ophthalmic solution) 0.03%

allergan singapore pte. ltd. - bimatoprost - solution, sterile - 0.3mg/ml

VALLERGAN Tablets 10 Milligram Airija - anglų - HPRA (Health Products Regulatory Authority)

vallergan tablets 10 milligram

sanofi-aventis ireland limited - trimeprazine tartare - tablets - 10 milligram

VALLERGAN 10 Milligram Tablets Airija - anglų - HPRA (Health Products Regulatory Authority)

vallergan 10 milligram tablets

sanofi-aventis ireland limited t/a sanofi - trimeprazine tartare - tablets - 10 milligram

Ganfort Europos Sąjunga - anglų - EMA (European Medicines Agency)

ganfort

allergan pharmaceuticals ireland - bimatoprost, timolol - glaucoma, open-angle, ocular hypertension - ophthalmologicals, - reduction of intraocular pressure (iop) in patients with open-angle glaucoma or ocular hypertension who are insufficiently responsive to topical beta-blockers or prostaglandin analogues.