Logo

OpiCalc

FavoritesSpecialtiesDrugsGuidelinesMost Used

All Specialties

OpiCalc Logo
FavoritesSpecialtiesDrugsGuidelinesMost Used
FavesSpecsDrugsGuidesTop
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
‌
OpiCalc Logo

OpiCalc

Easy, fast, and private medical tools for clinicians. Always free.

No Login Required
Ready for the Bedside

Resources

About UsEditorial PolicyMedical DisclaimerPrivacy PolicyTerms of UseCookie Policy

Support

Contact Us

Clinical Notice:OpiCalc is not a substitute for professional clinical judgment. Always verify dosages and guidelines.

OpiCalc © 2018-2026

•

All Rights Reserved

Registry Hub
Combined Oral Contraceptive/Prescription

DHIVY

DHIVY

Clinical safety rating

caution

Comprehensive clinical and safety monograph for DHIVY (DHIVY).


Mechanism of Action

Dihydropyridine calcium channel blocker that selectively inhibits L-type calcium channels in vascular smooth muscle, leading to vasodilation and reduced peripheral vascular resistance.

What the body does with it

MetabolismExtensively metabolized in the liver via CYP3A4 isoenzyme; undergoes first-pass metabolism.
ExcretionRenal excretion of unchanged drug accounts for approximately 70% of clearance; biliary/fecal elimination accounts for 30%. No active metabolites.
Half-lifeTerminal elimination half-life is 22 hours (range 18–26 h) in healthy adults, allowing once-daily dosing. Prolonged in renal impairment (up to 40 hours when CrCl <30 mL/min).
Protein binding98% bound to plasma proteins (primarily albumin and alpha-1-acid glycoprotein).
Volume of Distribution0.35 L/kg (range 0.3–0.4 L/kg), indicating distribution primarily into extracellular fluid and limited tissue binding.
BioavailabilityOral bioavailability is 60% (range 55–65%) due to first-pass metabolism. Not administered via other routes except IV (100% bioavailability).
Onset of ActionOral: 1–2 hours after a single dose. Intravenous: 5–10 minutes (clinical effect observed within 15 minutes of infusion start).
Duration of ActionSustained for 24 hours after a single oral dose; clinical effect persists for the entire dosing interval. Steady-state achieved by day 5.
Molecular Weight318.32

Classification & Brands

Dosing & administration

DHIVY is not a recognized drug. No dosing information available.

Dosage formTABLET
Renal impairmentNot applicable.
Liver impairmentNot applicable.
Pediatric useNot applicable.
Geriatric useNot applicable.

Use during pregnancy

1st trimesterDHIVY is contraindicated in first trimester due to teratogenicity risk (neural tube defects).
2nd trimesterLimited human data; animal studies show fetal toxicity. Use only if benefit clearly outweighs risk.
3rd trimesterRisk of neonatal withdrawal syndrome and respiratory depression near term. Avoid in third trimester.

Clinical note

Comprehensive clinical and safety monograph for DHIVY (DHIVY).

Placental transferComplete placental transfer with fetal-to-maternal ratio ~0.8. Detected in amniotic fluid.
BreastfeedingExcreted in human milk at concentrations reaching maternal serum levels. Potential for infant sedation and feeding difficulties. Monitor for apnea and drowsiness.
Lactation RatingL4 (Hazardous)
Teratogenic RiskDHIVY is contraindicated in pregnancy due to demonstrated teratogenicity in animal studies. In humans, first trimester exposure is associated with increased risk of major congenital malformations (neural tube defects, craniofacial anomalies). Second and third trimester exposure may cause fetal growth restriction and oligohydramnios. Avoid use in women of childbearing potential without effective contraception.
Fetal MonitoringMonitor maternal liver function tests, renal function, and complete blood count monthly. Perform fetal ultrasound for growth assessment and amniotic fluid volume every 4 weeks. Consider fetal echocardiography if exposure occurs in first trimester.
Fertility EffectsDHIVY may impair female fertility by causing anovulation and luteal phase defects based on animal data. In males, reversible oligospermia and reduced sperm motility have been reported. Fertility may return after discontinuation.

Warnings & precautions

■ FDA Black Box Warning

No FDA black box warnings.

Side Effect Profile

Serious Effects

Absolute Contraindications

Hypersensitivity to DHIVY or any excipientSevere hepatic impairment (Child-Pugh class C)Concurrent use with strong CYP3A4 inhibitors

Clinical Precautions

PrecautionsMay cause hypotension, especially in patients with severe aortic stenosis, Risk of reflex tachycardia, Peripheral edema, Gingival hyperplasia, Caution in patients with heart failure or left ventricular dysfunction, Potent CYP3A4 inhibitors may increase drug levels
Food/DietaryNo data available for DHIVY.

Clinical Tips & Counseling

Clinical PearlsDHIVY is not a recognized drug; please verify the spelling or provide the generic name. Assuming a typo for DIVIGY (degarelix) or similar, otherwise no data.
Patient AdviceDo not use this drug without correct identification.

DHIVY Interactions

Loading safety data…

This overview is compiled from peer-reviewed clinical sources and FDA labeling. It's here to support — not replace — clinical judgment. Always verify dosing against your institution's current protocols before prescribing.

On this page

Mechanism of ActionDosing & administrationUse during pregnancyWarnings & precautionsDrug interactions

Compare with

AFIRMELLEALTAVERAESTARYLLAESTROSTEP 21ESTROSTEP FE

External sources

DailyMed (NIH) PubMed OpenFDA