VIENOMET TABLETS 2MG Singapore - English - HSA (Health Sciences Authority)

vienomet tablets 2mg

abbott laboratories (singapore ) private limited - dienogest - tablet - dienogest 2mg

ABIRATERONE- abiraterone acetate tablet United States - English - NLM (National Library of Medicine)

abiraterone- abiraterone acetate tablet

msn laboratories private limited - abiraterone acetate (unii: em5ocb9yj6) (abiraterone - unii:g819a456d0) - abiraterone acetate tablets are indicated in combination with prednisone for the treatment of patients with • metastatic castration-resistant prostate cancer (crpc) • metastatic high-risk castration-sensitive prostate cancer (cspc) none. risk summary the safety and efficacy of abiraterone acetate have not been established in females. based on findings from animal studies and the mechanism of action, abiraterone acetate can cause fetal harm and potential loss of pregnancy. there are no human data on the use of abiraterone acetate in pregnant women. in animal reproduction studies, oral administration of abiraterone acetate to pregnant rats during organogenesis caused adverse developmental effects at maternal exposures approximately ≥ 0.03 times the human exposure (auc) at the recommended dose (see data). data animal data in an embryo-fetal developmental toxicity study in rats, abiraterone acetate caused developmental toxicity when administered at oral doses of 10, 30 or 100 mg/kg/day

RYTMONORM TABLET 150 mg Singapore - English - HSA (Health Sciences Authority)

rytmonorm tablet 150 mg

abbott laboratories (singapore ) private limited - propafenone hcl - tablet, film coated - 150 mg - propafenone hcl 150 mg

Voriconazole New Zealand - English - Medsafe (Medicines Safety Authority)

voriconazole

arrotex pharmaceuticals (nz) limited - voriconazole 200mg - film coated tablet - 200 mg - active: voriconazole 200mg excipient: colloidal silicon dioxide croscarmellose sodium lactose magnesium stearate maize starch opadry white 33k18618 povidone pregelatinised maize starch - voriconazole is indicated for treatment of the following fungal infections: · invasive aspergillosis. · serious candida infections (including c. krusei), including oesophageal and systemic candida infections (hepatosplenic candidiasis, disseminated candidiasis, candidaemia). · serious fungal infections caused by scedosporium spp. and fusarium spp. · other serious fungal infections, in patients intolerant of, or refractory to, other therapy.

Voriconazole New Zealand - English - Medsafe (Medicines Safety Authority)

voriconazole

arrotex pharmaceuticals (nz) limited - voriconazole 50mg - film coated tablet - 50 mg - active: voriconazole 50mg excipient: colloidal silicon dioxide croscarmellose sodium lactose magnesium stearate maize starch opadry white 33k18618 povidone pregelatinised maize starch - voriconazole is indicated for treatment of the following fungal infections: · invasive aspergillosis. · serious candida infections (including c. krusei), including oesophageal and systemic candida infections (hepatosplenic candidiasis, disseminated candidiasis, candidaemia). · serious fungal infections caused by scedosporium spp. and fusarium spp. · other serious fungal infections, in patients intolerant of, or refractory to, other therapy.

UNMASKED CREAM Canada - English - Health Canada

unmasked cream

flageoli limited - sulfur - cream - 8% - sulfur 8% - keratolytic agents

Stieprox Liquid New Zealand - English - Medsafe (Medicines Safety Authority)

stieprox liquid

glaxosmithkline nz limited - ciclopirox olamine 1.5%{relative};  ;  ; ciclopirox olamine 1.5%{relative} - shampoo - 1.5% w/w - active: ciclopirox olamine 1.5%{relative}     excipient: citric acid monohydrate cocamide diolamine cocamidopropyl betaine dibasic sodium phosphate dodecahydrate hexylene glycol oleyl alcohol fruitier timotei af 17050 fragrance polyquaternium-10 polysorbate 80 purified water sodium laureth sulfate active: ciclopirox olamine 1.5%{relative} excipient: citric acid cocamide diolamine cocamidopropyl betaine dibasic sodium phosphate dodecahydrate hexylene glycol fragrance timotei af 17050 oleyl alcohol polyquaternium-10 polysorbate 80 purified water sodium laureth sulfate

Metformin New Zealand - English - Medsafe (Medicines Safety Authority)

metformin

ipca pharma (nz) pty limited - metformin hydrochloride 850mg;  ;  ; metformin hydrochloride 850mg - film coated tablet - 850 mg - active: metformin hydrochloride 850mg     excipient: colloidal silicon dioxide hypromellose macrogol 6000 magnesium stearate maize starch povidone propylene glycol purified talc sodium starch glycolate titanium dioxide active: metformin hydrochloride 850mg excipient: colloidal silicon dioxide hypromellose macrogol 6000 magnesium stearate maize starch povidone propylene glycol purified talc sodium starch glycolate titanium dioxide - treatment of type 2 diabetes mellitus in adults, particularly in overweight patients, when dietary management and exercise alone does not result in adequate glycaemic control. metformin may be used as initial treatment or in sulfonylurea failures either alone or in combination with a sulfonylurea and other oral agents.

HALOPERIDOL lactate injection solution United States - English - NLM (National Library of Medicine)

haloperidol lactate injection solution

pfizer laboratories div pfizer inc - haloperidol lactate (unii: 6387s86pk3) (haloperidol - unii:j6292f8l3d) - haloperidol 5 mg in 1 ml