REMS
Contraindicated in:
Pregnancy
;Use Cautiously in:
Women of reproductive potential
;CV: hypotension, chest pain, edema
F and E: hyperkalemia
GI: abdominal pain, diarrhea, nausea
GU: renal impairment
MS: arthralgia, back pain
Neuro: dizziness, fatigue, headache, dizziness, fatigue, headache
Misc: ANGIOEDEMA
Drug-drug:
Hypertension
Hepatic Impairment
Therapeutic Classification: antihypertensives
Pharmacologic Classification: angiotensin II receptor antagonists
Absorption: Candesartan cilexetil is a prodrug that is converted to candesartan (the active component); 15% bioavailability of candesartan.
Distribution: Minimally distributed to tissues.
Protein Binding: >99%.
Half-Life: 9 hr.
May cause fetal harm. Advise women of reproductive potential to use effective contraception, notify health care provider immediately if pregnancy is planned or suspected, and avoid breastfeeding. Candesartan should be discontinued as soon as possible when pregnancy is detected. Conduct serial ultrasound exams in pregnant patients exposed to candesartan; may cause oligohydramnios. Monitor infants exposed to candesartan in utero for hypotension, oliguria, and hyperkalemia. If oliguria or hypotension occurs, support BP and renal perfusion. Exchange transfusions or dialysis may be required as a means of reversing hypotension and/or substituting for disordered renal function.
NDC Code