Drug profile
Carvedilol
Adult, child, renal, hepatic, pregnancy and breastfeeding information, with the source named on every line.
DRUG INFORMATION
ADULT
- ( 2 ) Heart failure: Start at 10 mg once daily and increase to 20 mg, 40 mg, and
then 80 mg once daily over intervals of at least 2 weeks.
Source: US FDA label for carvedilol (Carvedilol Phosphate), section 'dosage and
administration', retrieved 2026-08-29
- ( 2.1 ) Left ventricular dysfunction following myocardial infarction: Start at 20
mg once daily and increase to 40 mg then 80 mg once daily after intervals of 3 to
10 days.
Source: US FDA label for carvedilol (Carvedilol Phosphate), section 'dosage and
administration', retrieved 2026-08-29
- ( 2.2 ) Hypertension: Start at 20 mg once daily and increase if needed for blood
pressure control to 40 mg then 80 mg once daily over intervals of 1 to 2 weeks.
Source: US FDA label for carvedilol (Carvedilol Phosphate), section 'dosage and
administration', retrieved 2026-08-29
CHILD
- Carvedilol phosphate extended-release capsules are intended for once-daily
administration. Patients controlled with immediate-release carvedilol tablets
alone or in combination with other medications may be switched to carvedilol
phosphate extended-release capsules based on the total daily doses shown in Table
1. Table 1.
Source: This line points to a numbered table that this card does not show - read
that table in the label before you dose. US FDA label for carvedilol (Carvedilol
Phosphate), section 'dosage and administration', retrieved 2026-08-29
RENAL IMPAIRMENT
- Patients at risk appear to be those with low blood pressure (systolic blood
pressure less than 100 mm Hg), ischemic heart disease and diffuse vascular
disease, and/or underlying renal insufficiency.
Source: US FDA label for carvedilol (Carvedilol Phosphate), section 'warnings and
cautions', retrieved 2026-08-29
HEPATIC IMPAIRMENT
- Concomitant administration with a diuretic can be expected to produce additive
effects and exaggerate the orthostatic component of carvedilol action. 2.4 Hepatic
Impairment Carvedilol phosphate extended-release capsules should not be given to
patients with severe hepatic impairment [see Contraindications (4) ] .
Source: US FDA label for carvedilol (Carvedilol Phosphate), section 'dosage and
administration', retrieved 2026-08-29
PREGNANCY
- Risk Summary Available data regarding use of carvedilol phosphate extended-release
capsules in pregnant women are insufficient to determine whether there are drug-
associated risks of adverse developmental outcomes.
Source: US FDA label for carvedilol (Carvedilol Phosphate), section 'pregnancy',
retrieved 2026-08-29
- There are risks to the mother and fetus associated with poorly controlled
hypertension in pregnancy.
Source: US FDA label for carvedilol (Carvedilol Phosphate), section 'pregnancy',
retrieved 2026-08-29
- The use of beta blockers during the third trimester of pregnancy may increase the
risk of hypotension, bradycardia, hypoglycemia, and respiratory depression in the
neonate [see Clinical Considerations ] .
Source: US FDA label for carvedilol (Carvedilol Phosphate), section 'pregnancy',
retrieved 2026-08-29
BREASTFEEDING
- Risk Summary There are no data on the presence of carvedilol in human milk, the
effects on the breastfed infant, or the effects on milk production.
Source: US FDA label for carvedilol (Carvedilol Phosphate), section 'nursing
mothers', retrieved 2026-08-29
- Carvedilol is present in the milk of lactating rats.
Source: US FDA label for carvedilol (Carvedilol Phosphate), section 'nursing
mothers', retrieved 2026-08-29
- The developmental and health benefits of breastfeeding should be considered along
with the mother’s clinical need for carvedilol phosphate extended-release capsules
and any potential adverse effects on the breastfed infant from carvedilol
phosphate extended-release capsules or from the underlying maternal condition.
Source: US FDA label for carvedilol (Carvedilol Phosphate), section 'nursing
mothers', retrieved 2026-08-29