Article Contents ::
- 1 Details About Generic Salt :: Doxazosi
- 2 Main Medicine Class::
- 3 (DOX-uh-ZOE-sin MEH-suh-late) Cardura Tablets 1 mg Tablets 2 mg Tablets 4 mg Tablets 8 mg Cardura-1, Cardura-2, Cardura-4 Class: Antihypertensive, Antiadrenergic, peripherally acting
- 4 Drugs Class ::
- 5 Disclaimer ::
- 6 The Information available on this site is for only Informational Purpose , before any use of this information please consult your Doctor .Price of the drugs indicated above may not match to real price due to many possible reasons may , including local taxes etc.. These are only approximate indicative prices of the drug.
Details About Generic Salt :: Doxazosi
Main Medicine Class::
(DOX-uh-ZOE-sin MEH-suh-late)
Cardura
Tablets
1 mg
Tablets
2 mg
Tablets
4 mg
Tablets
8 mg
Cardura-1, Cardura-2, Cardura-4
Class: Antihypertensive, Antiadrenergic, peripherally acting
Drugs Class ::
Action Selectively blocks postsynaptic alpha-1-adrenergic receptors, resulting in dilation of arterioles and veins.
Indications for Drugs ::
Indications Treatment of hypertension, alone or in combination with other agents; treatment of benign prostatic hyperplasia (BPH).
Drug Dose ::
Route/Dosage
Hypertension Adults: Initial dose: PO 1 mg qd. Maintenance: Based on standing BP response, may increase to 2 mg and thereafter to 4, 8, and 16 mg.
Benign Prostatic Hyperplasia Adults: Initial dose: PO 1 mg/day. Maintenance: Increase to 2 mg, and thereafter to 4 and 8 mg once daily, which is the max dose for BPH. Recommended titration interval is 1 to 2 wk.
Contraindication ::
Contraindications Hypersensitivity to prazosin or terazosin.
Drug Precautions ::
Precautions
Pregnancy: Category C. Lactation: Excreted in breast milk. Children: Safety and efficacy not established. “First-dose” effect: Marked hypotension (especially orthostatic) and syncope may occur at 2 to 6 hr after first few doses, after reintroduction, with rapid increase in dosing or after addition of another antihypertensive. Hepatic impairment: Use drug with extreme caution. Lipids: Slight decrease in total serum cholesterol and LDL may occur as well as increase in HDL.
PATIENT CARE CONSIDERATIONS |
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Drug Side Effects ::
Adverse Reactions
CARDIOVASCULAR: Palpitations; orthostatic hypotension; hypotension; arrhythmia; chest pain. CNS: Depression; dizziness; decreased libido; sexual dysfunction; nervousness; paresthesia; somnolence; headache; anxiety; insomnia; asthenia; ataxia; hypertonia. DERMATOLOGIC: Pruritus; rash; sweating. EENT: Abnormal vision; conjunctivitis; tinnitus; rhinitis; epistaxis; pharyngitis. GI: Nausea; vomiting; dry mouth; diarrhea; constipation; abdominal discomfort or pain; flatulence. GU: Incontinence; polyuria. RESPIRATORY: Dyspnea. OTHER: Shoulder, neck, back or extremity pain; arthritis; joint or muscle pain; gout; arthralgia; vertigo; edema; facial edema; flushing.
Drug Mode of Action ::
Action Selectively blocks postsynaptic alpha-1-adrenergic receptors, resulting in dilation of arterioles and veins.
Drug Interactions ::
Interactions
None well documented.
Drug Assesment ::
Assessment/Interventions
- Obtain patient history, including drug history and any known allergies. Note any history of liver failure.
- Record patient’s weight daily.
- Monitor BP and pulse 2 to 6 hr after initial dose and each increase and daily throughout therapy.
- Monitor LFTs, CBC, cholesterol, LDL, HDL, BUN, creatinine, and triglycerides.
- Monitor I&O.
- Monitor for chest pain and arrhythmia. Notify health care provider if these signs are present.
- Monitor patient for nausea, vomiting, abdominal distention, or pain.
- Monitor for edema. Check patient’s feet and legs daily for swelling.
- Observe skin for rash or diaphoresis.
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Drug Storage/Management ::
Administration/Storage
- Have patient swallow tablet whole. Do not crush or allow patient to chew tablet.
- Give first dose at bedtime to decrease possibility of orthostatic hypotension, dizziness, and syncope.
- Store at room temperature.
Drug Notes ::
Patient/Family Education
- Remind patient to take tablets whole and to not crush or chew tablets.
- Teach patient how to take BP. Advise patient to monitor weekly and to notify health care provider if significant changes occur.
- Emphasize importance of reducing the following risk factors: smoking cessation, weight loss, discontinuation of dietary intake of fat, exercise.
- Caution patient not to discontinue medication, even if feeling well, unless directed by health care provider.
- Instruct patient to record weight 3 times/wk.
- Advise patient to report the following symptoms to health care provider: nausea, vomiting or diarrhea; dizziness; chest pain or palpitations; swelling of feet or ankles.
- Caution patient to avoid sudden position changes 2 to 6 hr after taking medication to prevent orthostatic hypotension and syncope.
- Advise patient that drug may cause drowsiness and to use caution while driving or performing other tasks requiring mental alertness.
- Instruct patient not to take OTC medications without consulting health care provider.