On the first day of travel, the first dose should be taken 30 to 60 minutes before the anticipated travel, and the second one should be taken 8 to 12 hours later, if necessary. Home +1-877-289-FEEL; Arts; Provigil and hormonal birth control; Took unisom instead of sleeping i am awake; LGBT ; Opinion +1-877 …

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Site users seeking medical advice about their specific situation should consult with their own physician. In order for us to create your customized HealthSavvy programs, we need a little more information about the health topic(s) that you are interested in. ), hydrocortisone sodium succinate(? This site does not dispense medical advice or advice of any kind. Promethazine (also called ­­­Phenergan®) is a medicine called an antiemetic. and formulary information changes. Philadelphia, PA: Wyeth Pharmaceuticals, Inc.; 2005 July.Promethazine Syrup [package insert]. )Administer by deep IM injection or by injection into tubing of running IV infusion solutionIV: Concentration <25 mg/mL; infusion rate not to exceed 25 mg/minStore at controlled room temperature; protect from freezingDiscard if particulate matter formation or discoloration occursAdding plans allows you to compare formulary status to other drugs in the same class.To view formulary information first create a list of plans. On subsequent days of travel, the first dose should be taken right after getting up in the morning, and the second one should be taken before the evening meal.A similar dosing regimen is recommended for children, except with a lower amount: Phenergan 12.5 to 25 mg twice daily. ), cefepime, cefoperazone, cefotetan, ceftizoxime(? PO/PR: 25 mg at bedtime or 12.5 mg before meals and at bedtime (dosage range, 6.25-12.5 mg q8hr)IV/IM: 25 mg; may be repeated in 2 hours when necessary; switch to PO as soon as possible25 mg PO/PR 30-60 minutes before departure and q8-12hr PRN; on succeeding travel days, 25 mg PO/PR every morning and every evening50 mg PO/PR on night before procedure or 25-50 mg IV/IM combined with reduced doses of analgesics and atropinelike drugs25-50 mg IV/IM/PO/PR combined with reduced doses of analgesics and atropinelike drugs25-50 mg IV/IM in early labor; may be increased to 25-75 mg q2-4hr after labor established; not to exceed two doses or up to 100 mg/day during labor≥2 years old: 25 mg PO/PR at bedtime or 12.5 mg q6hr; alternatively, 6.25-12.5 mg PO/PR q8hr≥2 years old: 0.25-1 mg/kg PO/PR q4-6hr PRN; not to exceed 25 mg ≥2 years: 12.5-25 mg PO/PR administered 30-60 minutes before departure and q8-12hr PRN or 0.5 mg/kg PO q12hr PRN Succeeding days of travel: 12.5-25 mg twice daily (upon arising or before evening meals)≥2 years: 1 mg/kg PO/PR with reduced dose of analgesic and appropriate dose of atropinelike drug ≥2 years: 12.5-25 mg with reduced dose of analgesic and appropriate dose of atropinelike drugIV administration can cause severe tissue injury, including burning, gangrene, or thrombophlebitis, necessitating fasciotomy, skin graft, or amputationSevere tissue injury can occur from perivascular extravasation, unintentional intra-arterial injection, and intraneuronal or perineuronal infiltrationDeep IM injection is preferred method of administrationIntra-arterial and SC administration are contraindicated25 mg/mL product may be administered by deep IM injection or IV infusion (at rate not to exceed 25 mg/min through flowing IV tubing)Monitor for signs and symptoms of potential tissue injury including burning or pain at site of injection, phlebitis, swelling, and blisteringDiscontinue IV infusion immediately if patient complains of pain during injectionRespiratory fatalities reported with use in children <2 years (use contraindicated); use lowest effective dose in children >2 years; avoid other drugs with respiratory depressant effectsNewborn/premature infants <2 years old (risk of potentially fatal respiratory depression)Treatment of lower respiratory tract symptoms, including asthmaUse caution in asthma, hepatic impairment, peptic ulcer disease, respiratory impairment, bone marrow suppression, anaphylaxis in susceptible individualsMay impair ability to drive or perform hazardous tasksMay impair core body temperature regulation; caution when taking medications with anticholinergic effects, heat exposure, or strenuous exerciseDepresses hypothalamic thermoregulatory mechanism; exposure to extreme temperatures may cause hypo- or hyperthermiaMay alter cardiac conduction (life-threatening arrhythmias reported)Antiemetic effect may obscure toxicity of chemotherapeutic drugsMonitor closely in patients with cardiovascular disease, hepatic impairment, Reye syndrome, or history of sleep apneaHas anticholinergic effects; use with caution in patients with decreased gastrointestinal motility or obstructions (partial or complete), urinary retention, urinary obstructions, xerostomia, BPH, or visual problemsMay cause extrapyramidal symptoms including pseudoparkinsonism, acute dystonic reactions, tardive dyskinesia, and akathisiaNeuroleptic malignant syndrome reported with use; monitor for fever, muscle rigidity and/or autonomic instability, or mental status changesMay cause orthostatic hypotension; use caution in patients at risk of experiencing hypotensive episodes (cardiovascular disease, cerebrovascular disease, hypovolemia or taking medications that may predispose to bradycardia or hypotension)Pyloroduodenal obstruction, stenosing peptic ulcer disease, bladder neck obstructionAnticholinergic effects of promethazine may exacerbate condition in patients with narrow-angle glaucoma or myasthenia gravisLactation: Not known whether drug crosses into breast milk; discontinue drug, or do not nurseA: Generally acceptable.
Promethazine topical gel is a way of giving your child this nausea medicine.


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