synastone 50mg/2ml solution for injection ampoules
auden mckenzie (pharma division) ltd - methadone hydrochloride - solution for injection - 25mg/1ml
synastone 10mg/1ml solution for injection ampoules
auden mckenzie (pharma division) ltd - methadone hydrochloride - solution for injection - 10mg/1ml
synastone 50mg/5ml solution for injection ampoules
auden mckenzie (pharma division) ltd - methadone hydrochloride - solution for injection - 10mg/1ml
uromitexan 400 mg injection
baxter healthcare south africa (pty) ltd - mesna a - injection - 400 mg - each 1 ml injection contains mesna a 100 mg
naltrexone hydrochloride tablets usp
sterinova inc. - naltrexone hydrochloride - tablet - 50mg - naltrexone hydrochloride 50mg - opiate antagonists
uromitexan 400 mg
megapharm ltd - mesna - solution for injection - mesna 400 mg/vial - mesna - prevention of urinary passage toxicity of oxazaphosphorines (ifosfamide ,cyclophosphamide, trofosamide), in particular in high-risk patients with previous radiation therapy in the area of the lesser pelvis, cystitis with previous ifosfamide, cyclophosphamide or trofosamide , urinary passage diseases in anamnesis.
uromitexan 1g/10ml solution for injection ampoules
baxter healthcare ltd - mesna - solution for injection - 100mg/1ml
uromitexan 400mg/4ml solution for injection ampoules
baxter healthcare ltd - mesna - solution for injection - 100mg/1ml
naltrexone 50mg tablets
aop orphan ltd - naltrexone hydrochloride - oral tablet - 50mg
contrave- naltrexone hydrochloride and bupropion hydrochloride tablet, film coated, extended release
a-s medication solutions - naltrexone hydrochloride (unii: z6375yw9sf) (naltrexone - unii:5s6w795cqm), bupropion hydrochloride (unii: zg7e5poy8o) (bupropion - unii:01zg3tpx31) - naltrexone hydrochloride 8 mg - contrave is indicated as an adjunct to a reduced-calorie diet and increased physical activity for chronic weight management in adults with an initial body mass index (bmi) of: limitations of use: pregnancy category x risk summary contrave is contraindicated during pregnancy, because weight loss offers no potential benefit to a pregnant woman and may result in fetal harm. if this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard of maternal weight loss to the fetus. clinical considerations a minimum weight gain, and no weight loss, is currently recommended for all pregnant women, including those who are already overweight or obese, due to the obligatory weight gain that occurs in maternal tissues during pregnancy. human data there are no adequate and well-controlled studies of contrave in pregnant women. in clinical studies, 21 (0.7%) of 3,024 women became pregnant while taking contrave: 11 carried to term and gave b