| |
|

| TERAZOSIN-HAKIM |
| :: Antihypertensive, Benign prostatic hyperplasia therapy agent :: |
|
Tab. 2 , 5 mg |
|
|
|
|
|
|
|
Pharmacologic category
Alpha 1 blocker; Antihypertensive; Benign prostatic hyperplasia therapy agent.
Mechanism of action
Terazosin has a peripheral post-synaptic alpha 1-blocking action. Terazosin produces vasodilation and reduces peripheral resistance but generally has little effect on cardiac output.Antihypertensive effect with chronic dosing is usually not accompanied by reflex tachycardia . Relaxation of smooth muscle in the bladder neck, prostate and prostate capsule produced by alpha 1-adrenergic blockade results in a reduction in urethral resistance and pressure, bladder outlet resistance and urinary symptoms.
Indications
Mild to moderate hypertension; Benign prostatic hyperplasia (BPH).
Side/Adverse effects
a- > 10 %: Dizziness; Headache; Muscle weakness
b- 1% to 10%: Edema; Palpitations; Chest pain ; Peripheral edema ; Orthostatic hypotension; Tachycardia; Fatigue; Nervousness; Drowsiness; Dry mouth; Urinary incontinence; Blurred vision; Dyspnea; Nasal congestion
c- <1% (Limited to important or life – threatening ): Allergic reactions; Anaphylaxis; Atrial fibrillation; Priapism; Sexual dysfunction; Syncope; Thrombocytopenia.
Contraindications
Hypersensitivity to quinazolines ( doxazosin, prazosin, terazosin) or any component of the formulations.
Warnings / Precautions
Terazosin can cause significant orthostatic hypotension and syncope,especially with first dose. Prostate cancer should be ruled out before starting for BPH. Anticipate a similar effect if therapy is interrupted for a few days , if dosage is rapidly increased , or if another antihypertensive drug is introduced.
Pregnancy
FDA pregnancy category C . Adequate and well- controlled studies in humans have not been done.
Breast–Feeding
It is not known whether terazosin is distributed into breast milk . However , problems in humans have not been documented.
Drug Interactions
Hypotensive effect of Terazosin may be increased by ACE inhibitors, beta – blockers and calcium channel blockers. NSAIDs , especially indomethacin may antagonize the antihypertensive effect of terazosin by inhibiting renal prostaglandin synthesis and/or by causing sodium and fluid retention . Antihypertensive effects of terazosin may be reduced when it is used concurrently with sympathomimetics . Concurrent use of terazosin antagonizes the peripheral vasoconstriction produced by high doses of dopamine. Concurrent use of terazosin may decrease the pressor response to ephedrine . Concurrent use of terazosin may block the alpha – adrenergic effects of epinephrine , possibly resulting in severe hypotension and tachycardia . Concurrent use of terazosin usually decreases the pressor effect of metaraminol . Prior administration of terazosin may decrease the pressor effect and shorten the duration of action of methoxamine and phenylephrine. Blood pressure – lowering effects of sildenafil and vardenafil are additive;therefore use of vardenafil is contraindicated and use of sildenafil is recommended with extreme caution during treatment with terazosin.
Monitoring Parameters
Standing and sitting /supine blood pressure , especially following the initial dose at 2-4 hours following the dose ; urinary symptoms.
Dietary Considerations
Terazosin may be taken without regard to meals.
Administration and dosage
-
Usual adult and adolescent dose:
Antihypertensive – Initial : Oral , 1 mg once a day , at bedtime.
Maintenance: Oral , adjusted gradually to meet individual requirement , usually 1 to 5 mg once a day.
Note: If the antihypertensive effect is not maintained for a full 24 hours , twice daily dosing may be more effective.
Benign prostatic hyperplasia – Initial: Oral , 1 mg once a day . at bedtime.
Maintenance: Oral , adjusted gradually up to 5 to 10 mg once a day, Doses of 10 mg once a day are generally required for an adequate response.
- Usual adult prescribing limits: Daily doses higher than 20 mg usually do not have increased efficacy.
- Usual pediatric dose: Safety and efficacy have not been established.
How Supplied
Tablet 2 mg, 5 mg.
Storage
Store below 40°C (104°F), preferably between 15 and 30°C (59 and 86°F).
References
- USP DI, 2004
- Up To Date, Vol. 13.1 (2005)
- Martindale, The Complete Drug Reference, 33 rd edition 2002
|