Hydralazine (injection)
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Gerald Chi
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Overview
Hydralazine (injection) is a vasodilator that is FDA approved for the {{{indicationType}}} of severe essential hypertension. Common adverse reactions include chest pain, palpitations, tachycardia, diarrhea, loss of appetite, nausea, vomiting, and headache.
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
Hypertension
- When there is urgent need, therapy in the hospitalized patient may be initiated intramuscularly or as a rapid intravenous bolus injection directly into the vein. Hydralazine hydrochloride injection should be used only when the drug cannot be given orally.
- Certain patients (especially those with marked renal damage) may require a lower dose. Blood pressure should be checked frequently. It may begin to fall within a few minutes after injection, with the average maximal decrease occurring in 10 to 80 minutes. In cases where there has been IICPincreased intracranial pressure, lowering the blood pressure may increase cerebral ischemia. Most patients can be transferred to oral hydralazine hydrochloride within 24 to 48 hours.
- The product should be used immediately after the vial is opened. It should not be added to infusion solutions. Hydralazine hydrochloride injection may discolor upon contact with metal; discolored solutions should be discarded.
- Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
- Dosing Information
- 20–40 mg IV/IM, repeated as necessary.
Off-Label Use and Dosage (Adult)
Guideline-Supported Use
There is limited information regarding Off-Label Guideline-Supported Use of Hydralazine (injection) in adult patients.
Non–Guideline-Supported Use
Mitral and Aortic Incompetence
- Dosing Information
- 37–225 mg/day[1]
Pulmonary Hypertension
- Dosing Information
- 0.15–0.3 mg/kg[2]
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
Hypertension
- Safety and effectiveness in pediatric patients have not been established in controlled clinical trials, although there is experience with the use of hydralazine hydrochloride in children.
- Dosing Information
- The usual recommended parenteral dosage, administered intramuscularly or intravenously, is 1.7 to 3.5 mg/kg of body weight daily, divided into four to six doses.
Off-Label Use and Dosage (Pediatric)
Guideline-Supported Use
There is limited information regarding Off-Label Guideline-Supported Use of Hydralazine (injection) in pediatric patients.
Non–Guideline-Supported Use
There is limited information regarding Off-Label Non–Guideline-Supported Use of Hydralazine (injection) in pediatric patients.
Contraindications
- Hypersensitivity to hydralazine
- Coronary artery disease
- Mitral valvular rheumatic heart disease
Warnings
Description
Adverse Reactions
Clinical Trials Experience
There is limited information regarding Clinical Trial Experience of Hydralazine (injection) in the drug label.
Central Nervous System
Cardiovascular
Respiratory
Gastrointestinal
Hypersensitivity
Miscellaneous
Postmarketing Experience
There is limited information regarding Postmarketing Experience of Hydralazine (injection) in the drug label.
Central Nervous System
Cardiovascular
Respiratory
Gastrointestinal
Hypersensitivity
Miscellaneous
Drug Interactions
- Drug
- Description
Use in Specific Populations
Pregnancy
- Pregnancy Category
- Australian Drug Evaluation Committee (ADEC) Pregnancy Category
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Hydralazine (injection) in women who are pregnant.
Labor and Delivery
There is no FDA guidance on use of Hydralazine (injection) during labor and delivery.
Nursing Mothers
There is no FDA guidance on the use of Hydralazine (injection) with respect to nursing mothers.
Pediatric Use
There is no FDA guidance on the use of Hydralazine (injection) with respect to pediatric patients.
Geriatic Use
There is no FDA guidance on the use of Hydralazine (injection) with respect to geriatric patients.
Gender
There is no FDA guidance on the use of Hydralazine (injection) with respect to specific gender populations.
Race
There is no FDA guidance on the use of Hydralazine (injection) with respect to specific racial populations.
Renal Impairment
There is no FDA guidance on the use of Hydralazine (injection) in patients with renal impairment.
Hepatic Impairment
There is no FDA guidance on the use of Hydralazine (injection) in patients with hepatic impairment.
Females of Reproductive Potential and Males
There is no FDA guidance on the use of Hydralazine (injection) in women of reproductive potentials and males.
Immunocompromised Patients
There is no FDA guidance one the use of Hydralazine (injection) in patients who are immunocompromised.
Administration and Monitoring
Administration
Oral
Intravenous
Monitoring
There is limited information regarding Monitoring of Hydralazine (injection) in the drug label.
Condition1
Description
IV Compatibility
There is limited information regarding IV Compatibility of Hydralazine (injection) in the drug label.
Overdosage
Acute Overdose
Signs and Symptoms
Description
Management
Description
Chronic Overdose
There is limited information regarding Chronic Overdose of Hydralazine (injection) in the drug label.
Pharmacology
There is limited information regarding Hydralazine (injection) Pharmacology in the drug label.
Mechanism of Action
There is limited information regarding Hydralazine (injection) Mechanism of Action in the drug label.
Structure
There is limited information regarding Structure of Hydralazine (injection) in the drug label.
Pharmacodynamics
There is limited information regarding Pharmacodynamics of Hydralazine (injection) in the drug label.
Pharmacokinetics
There is limited information regarding Pharmacokinetics of Hydralazine (injection) in the drug label.
Nonclinical Toxicology
There is limited information regarding Nonclinical Toxicology of Hydralazine (injection) in the drug label.
Clinical Studies
There is limited information regarding Clinical Studies of Hydralazine (injection) in the drug label.
Condition1
Description
How Supplied
There is limited information regarding Hydralazine (injection) How Supplied in the drug label.
Storage
There is limited information regarding Hydralazine (injection) Storage in the drug label.
Images
Drug Images
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Package and Label Display Panel
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Patient Counseling Information
There is limited information regarding Patient Counseling Information of Hydralazine (injection) in the drug label.
Precautions with Alcohol
- Alcohol-Hydralazine (injection) interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.[3]
Brand Names
- Apresoline®
Look-Alike Drug Names
- Apresoline® — Priscoline®[4]
- hydrALAZINE — hydrOXYzine[4]
Drug Shortage Status
Price
References
The contents of this FDA label are provided by the National Library of Medicine.
- ↑ Jensen, T. (1983-05). "Treatment with hydralazine in mild to moderate mitral or aortic incompetence". European Heart Journal. 4 (5): 306–312. ISSN 0195-668X. PMID 6617676. Unknown parameter
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(help) - ↑ McGoon, M. D. (1983-12). "Haemodynamic response to intravenous hydralazine in patients with pulmonary hypertension". British Heart Journal. 50 (6): 579–585. ISSN 0007-0769. PMC 481463. PMID 6652000. Unknown parameter
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