CIPLA COLD & FLU DAY TABLETS Paracetamol 500 mg, Pseudoephedrine Hydrochloride 30mg and codeine phosphate hemihydrate 6mg uncoated tablets, blister pack Australia - engleză - Department of Health (Therapeutic Goods Administration)

cipla cold & flu day tablets paracetamol 500 mg, pseudoephedrine hydrochloride 30mg and codeine phosphate hemihydrate 6mg uncoated tablets, blister pack

cipla australia pty ltd - codeine phosphate hemihydrate, quantity: 6 mg; paracetamol, quantity: 500 mg; pseudoephedrine hydrochloride, quantity: 30 mg - tablet, uncoated - excipient ingredients: magnesium stearate; colloidal anhydrous silica; maize starch; sodium starch glycollate; microcrystalline cellulose; povidone - temporary symptomatic relief of rhinorrhoea, nasal congestion, headache, myalgia and fever in patient aged 12 years and over.

TERAZOSIN HYDROCHLORIDE- terazosin hydrochloride capsule
TERAZOSIN HYDROCHLORIDE capsule Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

terazosin hydrochloride- terazosin hydrochloride capsule terazosin hydrochloride capsule

aphena pharma solutions - tennessee, llc - terazosin hydrochloride (unii: d32s14f082) (terazosin - unii:8l5014xet7) - terazosin 1 mg - terazosin capsules are indicated for the treatment of symptomatic benign prostatic hyperplasia (bph). there is a rapid response, with approximately 70% of patients experiencing an increase in urinary flow and improvement in symptoms of bph when treated with terazosin capsules. the long-term effects of terazosin capsules on the incidence of surgery, acute urinary obstruction or other complications of bph are yet to be determined. terazosin capsules are also indicated for the treatment of hypertension. terazosin capsules can be used alone or in combination with other antihypertensive agents such as diuretics or beta-adrenergic blocking agents. terazosin capsules are contraindicated in patients known to be hypersensitive to terazosin hydrochloride.

SUDOGEST- pseudoephedrine hydrochloride tablet Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

sudogest- pseudoephedrine hydrochloride tablet

dispensing solutions, inc. - pseudoephedrine hydrochloride (unii: 6v9v2ryj8n) (pseudoephedrine - unii:7cuc9ddi9f) - pseudoephedrine hydrochloride 60 mg - nasal decongestant - temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies - temporarily relieves sinus congestion and pressure

SUDOGEST- pseudoephedrine hydrochloride tablet, film coated Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

sudogest- pseudoephedrine hydrochloride tablet, film coated

rebel distributors corp - pseudoephedrine hydrochloride (unii: 6v9v2ryj8n) (pseudoephedrine - unii:7cuc9ddi9f) - pseudoephedrine hydrochloride 60 mg - nasal decongestant - temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies - temporarily relieves sinus congestion and pressure

SUDOGEST- pseudoephedrine hydrochloride tablet Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

sudogest- pseudoephedrine hydrochloride tablet

rebel distributors corp - pseudoephedrine hydrochloride (unii: 6v9v2ryj8n) (pseudoephedrine - unii:7cuc9ddi9f) - pseudoephedrine hydrochloride 30 mg - nasal decongestant - temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies, and nasal congestion associated with sinusitis - temporarily relieves sinus congestion and pressure

BROMPHENIRAMINE MALEATE, PSEUDOEPHEDRINE HYDROCHLORIDE, AND DEXTROMETHORPHAN HYDROBROMIDE syrup Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

brompheniramine maleate, pseudoephedrine hydrochloride, and dextromethorphan hydrobromide syrup

taro pharmaceuticals u.s.a., inc. - brompheniramine maleate (unii: ixa7c9zn03) (brompheniramine - unii:h57g17p2fn), pseudoephedrine hydrochloride (unii: 6v9v2ryj8n) (pseudoephedrine - unii:7cuc9ddi9f), dextromethorphan hydrobromide (unii: 9d2rti9kyh) (dextromethorphan - unii:7355x3rots) - brompheniramine maleate 2 mg in 5 ml - brompheniramine maleate, pseudoephedrine hydrochloride, and dextromethorphan hydrobromide syrup is indicated for relief of coughs and upper respiratory symptoms, including nasal congestion, associated with allergy or the common cold. hypersensitivity to any of the ingredients. do not use in the newborn, in premature infants, in nursing mothers, or in patients with severe hypertension or severe coronary artery disease. do not use dextromethorphan in patients receiving monoamine oxidase (maoi) inhibitors (see drug interactions ). antihistamines should not be used to treat lower respiratory tract conditions including asthma.

EPHEDRINE SULFATE injection, solution Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

ephedrine sulfate injection, solution

endo usa, inc. - ephedrine sulfate (unii: u6x61u5zeg) (ephedrine - unii:gn83c131xs) - ephedrine sulfate 50 mg in 1 ml - ephedrine sulfate injection is indicated for the treatment of clinically important hypotension occurring in the setting of anesthesia. none r isk summary limited published data on the use of ephedrine sulfate are insufficient to determine a drug associated risk of major birth defects or miscarriage. however, there are clinical considerations [see clinical considerations] . animal reproduction studies have not been conducted with ephedrine sulfate. the estimated background risk of major birth defects and miscarriage for the indicated population is unknown.  all pregnancies have a background risk of birth defect, loss, or other adverse outcomes.  in the u.s. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively. c linical considerations fetal/neonatal adverse reactions cases of potential metabolic acidosis in newborns at delivery with maternal ephedrine exposure have been reported in the literature. these reports describe umbilical artery ph of ≤7.2 at the time of delivery [see clinical pharmacology 12.3] . monitoring of the newborn for signs and symptoms of metabolic acidosis may be required. monitoring of infant’s acid-base status is warranted to ensure that an episode of acidosis is acute and reversible. r isk summary limited published literature reports that ephedrine is present in human milk. however, no information is available on the effects of the drug on the breastfed infant or the effects of the drug on milk production. the developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for ephedrine sulfate injection and any potential adverse effects on the breastfed child from ephedrine sulfate injection or from the underlying maternal condition. safety and effectiveness in pediatric patients have not been established. clinical studies of ephedrine did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. other reported clinical experience has not identified differences in responses between the elderly and younger patients. in general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy. this drug is known to be substantially excreted by the kidney, and the risk of adverse reactions to this drug may be greater in patients with impaired renal function. because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function. ephedrine and its metabolite are excreted in urine. in patients with renal impairment, excretion of ephedrine is likely to be affected with a corresponding increase in elimination half-life, which will lead to slow elimination of ephedrine and consequently prolonged pharmacological effect and potentially adverse reactions. monitor patients with renal impairment carefully after the initial bolus dose for adverse events.

CVS HEALTH NON-DROWSY NASAL DECONGESTANT- pseudoephedrine hydrochloride pill Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

cvs health non-drowsy nasal decongestant- pseudoephedrine hydrochloride pill

westport pharmaceuticals - pseudoephedrine hydrochloride (unii: 6v9v2ryj8n) (pseudoephedrine - unii:7cuc9ddi9f) - pseudoephedrine hydrochloride 30 mg - purpose nasal decongestant uses - temporarily relieves nasal congestion due to the common cold, hay fever, or other upper respiratory allergies - temporarily relieves sinus congestion and pressure

NASAL DECONGESTANT- pseudoephedrine hydrochloride capsule, gelatin coated Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

nasal decongestant- pseudoephedrine hydrochloride capsule, gelatin coated

cvs pharmacy - pseudoephedrine hydrochloride (unii: 6v9v2ryj8n) (pseudoephedrine - unii:7cuc9ddi9f) - pseudoephedrine hydrochloride 30 mg - nasal decongestant if you are now taking a prescription monoamine oxidase inhibitor (maoi) (certain drugs for depression, psychiatric, or emotional conditions, or parkinson’s disease), or for 2 weeks after stopping the maoi drug. if you do not know if your prescription drug contains an maoi, ask a doctor or pharmacist before taking this product.

ALLERGY RELIEF D- cetirizine hcl, pseudoephedrine hcl tablet, extended release Statele Unite ale Americii - engleză - NLM (National Library of Medicine)

allergy relief d- cetirizine hcl, pseudoephedrine hcl tablet, extended release

cvs pharmacy - cetirizine hydrochloride (unii: 64o047ktoa) (cetirizine - unii:yo7261me24), pseudoephedrine hydrochloride (unii: 6v9v2ryj8n) (pseudoephedrine - unii:7cuc9ddi9f) - cetirizine hydrochloride 5 mg - antihistamine nasal decongestant