Displaying 1 - 14 of 14
Active Ingredient PHENYLEPHRINE
Therapeutic Class ALPHA ADRENERGIC AGONIST
Indications
Caution
Dose Range
Drug Interactions
Pregnancy
Breast Feeding
Active Ingredient ADRENALINE
Therapeutic Class ALPHA & BETA ADRENERGIC AGONIST
Indications Acute bronchospasm. Emergency treatment of asthma and anaphylaxis, cardiac arrest.
Caution Cardiac arrhythmias, tachycardia, tremor, anxiety . Avoid in the elderly and patients with heart disease.
Dose Range 0.5-1mg s.c. or i.m.
Drug Interactions
Pregnancy May reduce placental perfusion and cause tachycardia, cardiac irregularities, an More ...
Breast Feeding Present in milk but unlikely to be harmful as poor oral bioavailability.
Active Ingredient EPHEDRINE HYDROCHLORIDE
Therapeutic Class ALPHA & BETA ADRENERGIC AGONIST
Indications Reversal of hypotension from spinal or epidural anaesthesia
Caution Anginal pain; anxiety; arrhythmias; flushing; headache;
hypersalivation.
Dose Range 3-6 mg every 3-4 minutes (max. p er dose 9 mg), adjusted according to response, injection solution to contain ephedrine hydrochloride 3 mg/ml; maximum 30 mg p er course.
Drug Interactions
Pregnancy Increased fetal heart rate has been reported. Use with caution during pregnancy.
Breast Feeding
Active Ingredient NORADRENALINE
Therapeutic Class ALPHA & BETA ADRENERGIC AGONIST
Indications
Caution
Dose Range
Drug Interactions
Pregnancy
Breast Feeding
Active Ingredient PSEUDOEPHEDRINE
Therapeutic Class ALPHA & BETA ADRENERGIC AGONIST
Indications Symptomatic relief of nasal congestion.
Caution Tachycardia, anxiety, restlessness, and insomnia.
Dose Range Adults and children over 12 years: 60mg every 4-6 hours to a maximum of 4 doses in 24 hours; patients with renal dysfunction should have dose adjustments. Pediatric: 6-12 years: 30mg 3-4 times daily.
Drug Interactions
Pregnancy Pseudoephedrine should be avoided during pregnancy because of the severity of th More ...
Breast Feeding May suppress lactation; avoid if lactation is not well established or if milk pr More ...
Active Ingredient TAMSULOSIN MR
Therapeutic Class SELECTIVE ALPHA 1 ADRENERGIC BLOCKING AGENTS
Indications Benign prostatic hyperlasia.
Caution Abnormal ejaculation, dizziness, arthalgia, headache, nausea, diarrhoea, rhinitis and slight reductions in hemoglobin have been reported. Food may decrease absorption of tamsulosin. Alterations in blo More ...
Dose Range The recommended oral dose for the treatment of benign prostatic hyperplasia is 0.4mg once daily,to be taken ½ hour after same meal daily. See BDS supply protocols pg. 11.
Drug Interactions
Pregnancy Use of tamsulosin is not approved for women.
Breast Feeding Use of tamsulosin is not approved for women.
Active Ingredient METHYLDOPA
Therapeutic Class CENTRAL ALPHA ANTAGONIST
Indications Hypertension.
Caution Rarely : Positive response to direct Coombs tests. Haemolytic anaemia, leukopenia, thrombocytopenia, hepatitis, gynaecomastia and lactation. Safe in asthmatics and pregnancy.Dose dependen More ...
Dose Range Adult: Initial dose: 250mg 2-3 times daily for 2 days, adjusted every
2 days to a maximum of 3g daily. Maintenance dose: 500mg-2g in 2-
4 divided doses. Pediatric: 10mg/kg in 2-4 divided doses initially , to a maximum of 65mg/kg or 3g whichever is less.
Drug Interactions
Pregnancy
Breast Feeding
Active Ingredient PRAZOSIN
Therapeutic Class ALPHA ADRENERGIC BLOCKING AGENTS
Indications Benign Prostatic Hypertrophy .
Caution To reduce incidence of syncope on first dose patient should be given
1mg at bedtime for firstfew doses. Dry mouth, drowsiness and nasal congestion. Dizziness, headache, lack of energy, weakness, palpi More ...
Dose Range Initially 500mcg twice daily for 3-7 days, subsequently adjusting accordingly to response. Maximum dose 2 mg twice daily.
Drug Interactions
Pregnancy Manufacturer advises use only when potential benefit outweighs risk.
Breast Feeding Use prazosin with caution in lactating women as it is distributed in breastmilk.
Active Ingredient TERAZOSIN
Therapeutic Class ALPHA ADRENERGIC BLOCKING AGENTS
Indications Benign prostatic hyperplasia.
Caution Dizziness, lethargy, edema, headache and fatigue.THE FIRST DOSE MUST BE TAKEN AT BEDTIME. Patient should be warned to lie down if symptoms such as dizziness, fatigue or sweating develop, and to rem More ...
Dose Range
Drug Interactions
Pregnancy Manufacturer advises use only when potential benefit outweighs risk.
Breast Feeding
Active Ingredient BRIMONIDINE
Therapeutic Class EENT ALPHA ADRENERGIC AGONISTS
Indications Ocular hypotension and glaucoma.
Caution Blurring. lid retraction, headache, fatigue, drowsiness. TO BE USED ONLY IN THOS E PATIENTS UNRESPONS IVE TO OTHER PREPARATIONS .
Dose Range 1 drop 3 times daily. See BDS supply protocols pg. 11.
Drug Interactions
Pregnancy
Breast Feeding
Active Ingredient ACARBOSE
Therapeutic Class ALPHA GLUCOSIDASE INHIBITORS
Indications
Caution
Dose Range
Drug Interactions
Pregnancy
Breast Feeding
Active Ingredient DUTASTERIDE
Therapeutic Class 5 ALPHA REDUCTASE INHIBITORS
Indications
Caution
Dose Range
Drug Interactions
Pregnancy
Breast Feeding
Active Ingredient DUTASTERIDE | TAMSULOSIN
Therapeutic Class 5 ALPHA REDUCTASE INHIBITORS
Indications
Caution
Dose Range
Drug Interactions
Pregnancy
Breast Feeding
Active Ingredient FINASTERIDE
Therapeutic Class 5 ALPHA REDUCTASE INHIBITORS
Indications Benign prostatic hyperplasia.
Caution Women/children should not handle tablets. Neoplasm of breast,
breast tenderness and swelling, ejaculation disorders erectile dy sfunction, rash, urticaria, depression, testicular pain and decreased More ...
Dose Range 5mg once daily.
Drug Interactions
Pregnancy
Breast Feeding