Acetylcysteine 600mg tablets United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

acetylcysteine 600mg tablets

alliance healthcare (distribution) ltd - acetylcysteine - oral tablet - 600mg

Acetylcysteine 600mg capsules United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

acetylcysteine 600mg capsules

alliance healthcare (distribution) ltd - acetylcysteine - oral capsule - 600mg

ACETAMINOPHEN INJECTION SOLUTION Canada - English - Health Canada

acetaminophen injection solution

avir pharma inc. - acetaminophen - solution - 10mg - acetaminophen 10mg - miscellaneous analgesics and antipyretics

Tri-Mag Supreme Powder Australia - English - Department of Health (Therapeutic Goods Administration)

tri-mag supreme powder

designs for health pty ltd - acetyl levocarnitine hydrochloride,glutamine,levomefolate glucosamine,magnesium amino acid chelate,magnesium glycerophosphate,magnesium orotate,mecobalamin (co-methylcobalamin),nicotinamide,pyridoxal 5-phosphate,riboflavin sodium phosphate,taurine,thiamine hydrochloride -

ACETYLCYSTEINE injection, solution United States - English - NLM (National Library of Medicine)

acetylcysteine injection, solution

sagent pharmaceuticals - acetylcysteine (unii: wyq7n0bpyc) (acetylcysteine - unii:wyq7n0bpyc) - acetylcysteine injection is indicated to prevent or lessen hepatic injury after ingestion of a potentially hepatotoxic quantity of acetaminophen in patients with acute ingestion or from repeated supratherapeutic ingestion (rsi). acetylcysteine is contraindicated in patients with a previous hypersensitivity reaction to acetylcysteine [see warnings and precautions (5.1)] . risk summary limited published case reports and case series of pregnant women exposed to acetylcysteine during various trimesters are not sufficient to inform any drug associated risk. delaying treatment of acetaminophen overdose may increase the risk of maternal or fetal morbidity and mortality [see clinical considerations]. reproduction studies in rats and rabbits following oral administration of acetylcysteine during the period of organogenesis at doses similar to the total intravenous dose (based on the body surface area) did not cause any adverse effects to the fetus. the estimated background risk of major birth defects and miscarriage