Moexipril/Hydrochlorothiazide
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Zaghw, M.D. [2], Amr Marawan, M.D. [3]
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Black Box Warning
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FETAL TOXICITY
See full prescribing information for complete Boxed Warning.
When pregnancy is detected, discontinue moexipril hydrochloride and hydrochlorothiazide tablets as soon as possible.
Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus.
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Overview
Moexipril/Hydrochlorothiazide is an Angiontensin converting enzyme inhibitor, Thiazide diuretic that is FDA approved for the {{{indicationType}}} of hypertension. There is a Black Box Warning for this drug as shown here. Common adverse reactions include dizziness (1.4% ), urinary tract infectious disease (greater than 1% ) and cough (3% ).
Adult Indications and Dosage
FDA-Labeled Indications and Dosage (Adult)
<h4>Condition 1</h4>
- Dosing Information
- (Dosage)
Off-Label Use and Dosage (Adult)
Pediatric Indications and Dosage
FDA-Labeled Indications and Dosage (Pediatric)
There is limited information regarding Moexipril/Hydrochlorothiazide FDA-Labeled Indications and Dosage (Pediatric) in the drug label.
Off-Label Use and Dosage (Pediatric)
Contraindications
There is limited information regarding Moexipril/Hydrochlorothiazide Contraindications in the drug label.
Warnings
|
FETAL TOXICITY
See full prescribing information for complete Boxed Warning.
When pregnancy is detected, discontinue moexipril hydrochloride and hydrochlorothiazide tablets as soon as possible.
Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus.
|
There is limited information regarding Moexipril/Hydrochlorothiazide Warnings' in the drug label.
Adverse Reactions
Clinical Trials Experience
There is limited information regarding Moexipril/Hydrochlorothiazide Clinical Trials Experience in the drug label.
Postmarketing Experience
There is limited information regarding Moexipril/Hydrochlorothiazide Postmarketing Experience in the drug label.
Drug Interactions
There is limited information regarding Moexipril/Hydrochlorothiazide Drug Interactions in the drug label.
Use in Specific Populations
Pregnancy
Pregnancy Category (FDA):
There is no FDA guidance on usage of Moexipril/Hydrochlorothiazide in women who are pregnant.
Pregnancy Category (AUS):
There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Moexipril/Hydrochlorothiazide in women who are pregnant.
Labor and Delivery
There is no FDA guidance on use of Moexipril/Hydrochlorothiazide during labor and delivery.
Nursing Mothers
There is no FDA guidance on the use of Moexipril/Hydrochlorothiazide in women who are nursing.
Pediatric Use
There is no FDA guidance on the use of Moexipril/Hydrochlorothiazide in pediatric settings.
Geriatic Use
There is no FDA guidance on the use of Moexipril/Hydrochlorothiazide in geriatric settings.
Gender
There is no FDA guidance on the use of Moexipril/Hydrochlorothiazide with respect to specific gender populations.
Race
There is no FDA guidance on the use of Moexipril/Hydrochlorothiazide with respect to specific racial populations.
Renal Impairment
There is no FDA guidance on the use of Moexipril/Hydrochlorothiazide in patients with renal impairment.
Hepatic Impairment
There is no FDA guidance on the use of Moexipril/Hydrochlorothiazide in patients with hepatic impairment.
Females of Reproductive Potential and Males
There is no FDA guidance on the use of Moexipril/Hydrochlorothiazide in women of reproductive potentials and males.
Immunocompromised Patients
There is no FDA guidance one the use of Moexipril/Hydrochlorothiazide in patients who are immunocompromised.
Administration and Monitoring
Administration
There is limited information regarding Moexipril/Hydrochlorothiazide Administration in the drug label.
Monitoring
There is limited information regarding Moexipril/Hydrochlorothiazide Monitoring in the drug label.
IV Compatibility
There is limited information regarding the compatibility of Moexipril/Hydrochlorothiazide and IV administrations.
Overdosage
There is limited information regarding Moexipril/Hydrochlorothiazide overdosage. If you suspect drug poisoning or overdose, please contact the National Poison Help hotline (1-800-222-1222) immediately.
Pharmacology
There is limited information regarding Moexipril/Hydrochlorothiazide Pharmacology in the drug label.
Mechanism of Action
There is limited information regarding Moexipril/Hydrochlorothiazide Mechanism of Action in the drug label.
Structure
There is limited information regarding Moexipril/Hydrochlorothiazide Structure in the drug label.
Pharmacodynamics
There is limited information regarding Moexipril/Hydrochlorothiazide Pharmacodynamics in the drug label.
Pharmacokinetics
There is limited information regarding Moexipril/Hydrochlorothiazide Pharmacokinetics in the drug label.
Nonclinical Toxicology
There is limited information regarding Moexipril/Hydrochlorothiazide Nonclinical Toxicology in the drug label.
Clinical Studies
There is limited information regarding Moexipril/Hydrochlorothiazide Clinical Studies in the drug label.
How Supplied
There is limited information regarding Moexipril/Hydrochlorothiazide How Supplied in the drug label.
Storage
There is limited information regarding Moexipril/Hydrochlorothiazide 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 Moexipril/Hydrochlorothiazide Patient Counseling Information in the drug label.
Precautions with Alcohol
Alcohol-Moexipril/Hydrochlorothiazide interaction has not been established. Talk to your doctor regarding the effects of taking alcohol with this medication.
Brand Names
There is limited information regarding Moexipril/Hydrochlorothiazide Brand Names in the drug label.
Look-Alike Drug Names
There is limited information regarding Moexipril/Hydrochlorothiazide Look-Alike Drug Names in the drug label.
Drug Shortage Status
Price
References
The contents of this FDA label are provided by the National Library of Medicine.