METOCLOPRAMIDE solution Ameerika Ühendriigid - inglise - NLM (National Library of Medicine)

metoclopramide solution

bryant ranch prepack - metoclopramide hydrochloride (unii: w1792a2rvd) (metoclopramide - unii:l4yeb44i46) - the use of metoclopramide oral solution is recommended for adults only. therapy should not exceed 12 weeks in duration. metoclopramide oral solution is indicated as short-term (4 to 12 weeks) therapy for adults with symptomatic, documented gastroesophageal reflux who fail to respond to conventional therapy. the principal effect of metoclopramide is on symptoms of post-prandial and daytime heartburn with less observed effect on nocturnal symptoms. if symptoms are confined to particular situations, such as following the evening meal, use of metoclopramide as single doses prior to the provocative situation should be considered, rather than using the drug throughout the day. healing of esophageal ulcers and erosions has been endoscopically demonstrated at the end of 12-week trial using doses of 15 mg 4 times daily. as there is no documented correlation between symptoms and healing of esophageal lesions, patients with documented lesions should be monitored endoscopically. metoclopramide is indicated for the relief of symptoms associated with acute and recurrent diabetic gastric stasis. the usual manifestations of delayed gastric emptying (e.g., nausea, vomiting, heartburn, persistent fullness after meals, and anorexia) appear to respond to metoclopramide within different time intervals. significant relief of nausea occurs early and continues to improve over a three-week period. relief of vomiting and anorexia may precede the relief of abdominal fullness by one week or more. metoclopramide should not be used whenever stimulation of gastrointestinal motility might be dangerous, e.g., in the presence of gastrointestinal hemorrhage, mechanical obstruction, or perforation. metoclopramide is contraindicated in patients with pheochromocytoma because the drug may cause a hypertensive crisis, probably due to release of catecholamines from the tumor. such hypertensive crises may be controlled by phentolamine. metoclopramide is contraindicated in patients with known sensitivity or intolerance to the drug. metoclopramide should not be used in epileptics or patients receiving other drugs which are likely to cause extrapyramidal reactions, since the frequency and severity of seizures or extrapyramidal reactions may be increased.

PHARMA-Q ADRENALINE INJECTION 1 mg/ml Lõuna-Aafrika Vabariik - inglise - South African Health Products Regulatory Authority (SAHPRA)

pharma-q adrenaline injection 1 mg/ml

pharma-q holdings (pty) ltd - injection - see ingredients - each 1 ml liquid contains epinephrine bitartrate 1,80 mg equivalent to epinephrine 1 mg

Midodrine Tillomed 2.5 mg tablets Iirimaa - inglise - HPRA (Health Products Regulatory Authority)

midodrine tillomed 2.5 mg tablets

tillomed pharma gmbh - midodrine hydrochloride - tablet - 2.5 milligram(s) - midodrine

Midodrine Tillomed 5 mg tablets Iirimaa - inglise - HPRA (Health Products Regulatory Authority)

midodrine tillomed 5 mg tablets

tillomed pharma gmbh - midodrine hydrochloride - tablet - 5 milligram(s) - midodrine

Mykronor 5 micrograms/ml, solution for injection/infusion Iirimaa - inglise - HPRA (Health Products Regulatory Authority)

mykronor 5 micrograms/ml, solution for injection/infusion

laboratoire aguettant - noradrenaline tartrate - solution for injection/infusion - 5 microgram(s)/millilitre - norepinephrine

Midodrine 2.5mg tablets Suurbritannia - inglise - MHRA (Medicines & Healthcare Products Regulatory Agency)

midodrine 2.5mg tablets

tillomed laboratories ltd - midodrine hydrochloride - oral tablet - 2.5mg