Acetylcysteine 200mg/ml Injection Malta - English - Medicines Authority

acetylcysteine 200mg/ml injection

central procurement & supplies unit - acetylcysteine - concentrate for solution for infusion - acetylcysteine 200 milligram(s)/millilitre - all other therapeutic products

Acetylcysteine 200mg/ml Injection Malta - English - Medicines Authority

acetylcysteine 200mg/ml injection

aurum pharmaceuticals limited bampton road, harold hill, romford essex, rm3 8ug, united kingdom - acetylcysteine - solution for infusion - acetylcysteine 200 mg/ml - all other therapeutic products

Acetylcysteine Concentrate for Soln for Inf 200mg/ml Malta - English - Medicines Authority

acetylcysteine concentrate for soln for inf 200mg/ml

p & d pharmaceuticals limited 38 woolmer way, bordon hampshire gu35 9qf, united kingdom - acetylcysteine - concentrate for solution for infusion - acetylcysteine 200 mg/ml - all other therapeutic products

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

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

acetylcysteine solution

fresenius kabi usa, llc - acetylcysteine (unii: wyq7n0bpyc) (acetylcysteine - unii:wyq7n0bpyc) - acetylcysteine solution, usp is indicated as adjuvant therapy for patients with abnormal, viscid, or inspissated mucous secretions in such conditions as: chronic bronchopulmonary disease (chronic emphysema, emphysema with bronchitis, chronic asthmatic bronchitis, tuberculosis, bronchiectasis and primary amyloidosis of the lung) acute bronchopulmonary disease (pneumonia, bronchitis, tracheobronchitis) pulmonary complications of cystic fibrosis tracheostomy care pulmonary complications associated with surgery use during anesthesia post-traumatic chest conditions atelectasis due to mucous obstruction diagnostic bronchial studies (bronchograms, bronchospirometry, and bronchial wedge catheterization) acetylcysteine is contraindicated in those patients who are sensitive to it. acetylcysteine solution, usp administered orally, is indicated as an antidote to prevent or lessen hepatic injury which may occur following the ingestion of a potentially hepatotoxic quantity of acetaminophen. it is essential to initiate trea

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

ACETYLCYSTEINE SANDOZ EFFERVESCENT TABLETS 600MG Singapore - English - HSA (Health Sciences Authority)

acetylcysteine sandoz effervescent tablets 600mg

sandoz singapore pte. ltd. - acetylcysteine - tablet, effervescent - 600mg - acetylcysteine 600mg

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

acetadote- acetylcysteine injection, solution

cumberland pharmaceuticals inc. - acetylcysteine (unii: wyq7n0bpyc) (acetylcysteine - unii:wyq7n0bpyc) - acetylcysteine 200 mg in 1 ml - acetadote 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). acetadote 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 for the indicated po