Article Contents ::
- 1 Details About Generic Salt :: Midodrin
- 2 Main Medicine Class:: Vassopressor,antihypotensive agent
- 3 (mid-OH-drean HIGH-droe-KLOR-ide) ProAmatine Class: Vassopressor/antihypotensive agent
- 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 :: Midodrin
Main Medicine Class:: Vassopressor,antihypotensive agent
(mid-OH-drean HIGH-droe-KLOR-ide)
ProAmatine
Class: Vassopressor/antihypotensive agent
Drugs Class ::
Action Activates arteriolar and venous a-adrenergic receptors resulting in an increase in vascular tone and elevation of blood pressure.
Indications for Drugs ::
Indications Treatment of symptomatic orthostatic hypotension in patients whose lives are considerably impaired despite standard clinical care, including support stockings, fluid expansion and lifestyle changes. Unlabeled use(s): Management of urinary incontinence.
Drug Dose ::
Route/Dosage
ADULTS: PO 10 mg tid during daytime hrs. Renal function impairment: Start with 2.5 mg/dose.
Contraindication ::
Contraindications Severe organic heart disease, acute renal failure, urinary retention, phenochromocytoma, thyrotoxicosis or in patients with persistent and excessive supine hypertension.
Drug Precautions ::
Precautions
Pregnancy: Category C. Lactation: Undetermined. Children: Safety and efficacy not established. Supine hypertension: Potentially most serious adverse reaction. Most common in patients with elevated pre-treatment supine systolic blood pressure (mean 170 mm/hg). Use is not recommended in patients with pre-treatment supine systolic blood pressure >180 mm/hg. Monitor supine and sitting blood pressures. Bradycardia: May occur due to vagal reflex. Use caution when coadministering with other agents that can reduce heart rate (eg, cardiac glycosides, b-blockers, psychopharmacologic agents). Urinary retention: Use with caution due to effect on a-adrenergic receptors of bladder neck. Renal function impairment: Use with caution. Initiate therapy with smaller doses. Hepatic function impairment: Use with caution. Diabetes: Use with caution.
PATIENT CARE CONSIDERATIONS |
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Drug Side Effects ::
Adverse Reactions
CV: Supine and sitting hypertension; bradycardia. CNS: Paresthesia; headache; confusion; nervousness; anxiety; confusion; abnormal thinking. DERM: Piloerection; scalp pruritis; rash. GI: Abdominal pain; dry mouth. GU: Dysuria (frequency, impaired micturation, urinary retention, urinary urgency). OTHER: Pain; chills; facial flushing; feeling of fullness/pressure in head.
Drug Mode of Action ::
Action Activates arteriolar and venous a-adrenergic receptors resulting in an increase in vascular tone and elevation of blood pressure.
Drug Interactions ::
Interactions
Vasoconstrictors (eg, dihydroergotamine, ephedrine, phenylephrine, phenylpropanolamine, pseudoephedrine): May enhance pressor effects of midodrine. Alpha-blocking agents (eg, prazosin, terazosin, doxazosin): May antagonize pressor effects of midodrine. Cardiac glycosides: May precipitate bradycardia, AV block or arrhythmia. Fludrocortisone: May exacerbate supine hypertension.
Drug Assesment ::
Assessment/Interventions
- Obtain patient history, including drug history and any known allergies. Note hepatic or renal impairment.
- Obtain necessary lab tests (eg, renal, liver) before initiating therapy.
- Monitor supine, sitting and standing blood pressure and pulse frequently during initiation of therapy.
- If supine hypertension noted, have patient sleep with head of bed elevated.
- If supine blood pressure noted to be > 180 mm/hg, withhold therapy and notify physician.
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Drug Storage/Management ::
Administration/Storage
- May be taken without regard to meal except evening dose.
- Dosing should be q 4 hrs during daylight hours while patient is upright. Administer first dose shortly before or upon arising, second dose at midday and third dose in late afternoon (no later than 6 pm).
- Doses may be given in 3 hour intervals, if required, to control symptoms, but not more frequently.
- Do not administer after evening meal or < 4 hrs before bedtime.
- Store at room temperature.
Drug Notes ::
Patient/Family Education
- Ensure that patient understands dosing schedule. Caution patient not to take dose after dinner or < 4 hours before bedtime.
- Medication can be taken without regard to meal except evening dose.
- Advise patient not to change the dose, dosing schedule or discontinue the medication without consulting with their physician.
- Ensure that patient has, and can use, a home blood pressure monitoring device. Advise patient to monitor blood pressure and pulse at regular intervals and notify physician if hypertension or bradycardia noted.
- Advise patient to elevate head of bed if supine hypertension noted.
- Educate patient regarding signs and symptoms of supine hypertension eg, cardiac awareness, pounding in ears, headache, blurred vision). Advise patient to discontinue medication and notify physician if noted.
- Caution patient to consult with their physician or pharmacist before taking other drugs, including otc medications.
- Advise female patients to notify their physician if they become pregnant or intend to become pregnant or are breastfeeding while taking this drug.
- Instruct patient to report the following symptoms: numbness or tingling; goosebumps; chills; flushing; feeling of fullness/pressure in head; eadache; confusion; nervousness; urinary problems.