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Fexofenadine

Antihistamine · Corticosteroid

Also known as Fexofenadine Hydrochloride, Allegra, Telfast

START
Confirm allergic rhinitis or urticaria diagnosis. Assess renal function. Counsel on taking with water only (NO fruit juice, antacids within 2 hours).
TYPICAL MAX
180 mg/day. Reduce to 60 mg/day if CrCl <80.
STOP IF
Severe hypersensitivity (anaphylaxis, angioedema), lack of efficacy after 2 weeks
WATCH
Renal function (dose adjustment), fruit juice consumption (counseling), symptoms of allergic condition
CDSCO approvedSchedule HJan AushadhiATC R06AX26
Dose laddermg/d
30start60titrate180ceiling
Renal dose adjustmenteGFR mL/min/1.73m²
FULLFull dose: …80REDUCEReduce: 60 mg once daily1590

KDIGO 2024 + manufacturer label

Pharmacokineticsplasma · t hours
1hONSET2.5hPEAK14.4h1dDURATION
ONSET
1h · Within 1 h
PEAK
2.5h · 2-3 h (oral)
14.4h · 14.4 h
DURATION
1d · 12-24 h (BID or daily dosing)
EXCRETION
~80% fecal; ~11% renal; minimal metabolism; P-gp substrate
route + CYP
INTERACTIONS
none in our sources
PREGNANCY
FDA PLLR: Animal studies showed no teratogenicity at doses up to 3x MRHD. Limited human data. Generally considered safe in pregnancy. Recommended as first-line antihistamine in pregnancy by ACOG.
FDA category + note
Available in India

742 branded formulations and 11 fixed-dose combinations. Look up specific brands in the Drugs workspace.

Jan Aushadhi — generic available at GoI pharmacies

Mechanism

Fexofenadine is a second-generation selective histamine H1-receptor antagonist. It competes with histamine for binding to H1 receptors on effector cells in the gastrointestinal tract, blood vessels, and respiratory tract, preventing histamine-mediated allergic responses (vasodilation, increased vascular permeability, smooth muscle contraction, itching). Unlike first-generation antihistamines, fexofenadine has minimal penetration of the blood-brain barrier due to active efflux by P-glycoprotein (MDR1) transporters at the blood-brain barrier, resulting in negligible sedation and anticholinergic effects. It is the active carboxylic acid metabolite of terfenadine (which was withdrawn due to QT prolongation).

Indications

Seasonal allergic rhinitis (hay fever)Chronic idiopathic urticaria (hives)Perennial allergic rhinitisAllergic conjunctivitis symptoms (off-label)Pruritus associated with allergic conditions (off-label)

Dosing

Adult
Allergic rhinitis/urticaria: 60 mg PO BID OR 180 mg PO once daily with water. Do NOT take with fruit juice (apple, orange, grapefruit — reduces absorption by ~40%).
Pediatric
2-11 years: 30 mg PO BID. 6 months-<2 years: 15 mg PO BID. 2-11 years (urticaria): 30 mg PO BID.
Renal adjustment
CrCl <80: Adults: 60 mg PO once daily. Children 6-11 years: 30 mg PO once daily. Children 2-5 years: 15 mg PO once daily. ESRD: clearance reduced 63%; AUC increased 2.8-fold — dose reduction essential.
Hepatic adjustment
No adjustment required (minimal hepatic metabolism).
Geriatric
No specific adjustment; consider renal function. Start at lower dose if CrCl <80.
Max dose
180 mg/day (normal renal function); 60 mg/day (CrCl <80)

Pharmacokinetics

Onset
Within 1 hour of administration.
Peak effect
Oral: peak plasma at 2-3 hours. Food does not significantly affect absorption (but fruit juice does).
Duration
12-24 hours (supports once- or twice-daily dosing).
Half-life
14.4 hours (adults); supports once-daily dosing at 180 mg.
Bioavailability
~30-40% (poor due to P-gp efflux and limited intestinal absorption). Grapefruit/orange/apple juice reduces absorption by ~40%.
Protein binding
60-70% (albumin and alpha-1-acid glycoprotein). Reduced to 56-68% in renal impairment.
Metabolism
Minimally metabolized (~5% of dose). Not a CYP substrate. Metabolites: methyl ester (3.6%) and MDL 4829 (1.5%) — both inactive. Intestinal flora may contribute to minimal metabolism.
Excretion
Feces: ~80% (unchanged and metabolites). Urine: ~11% (unchanged). Biliary excretion and intestinal secretion via P-gp and OATP transporters.

Contraindications

  • Hypersensitivity to fexofenadine or terfenadine

Side effects

Common
HeadacheDrowsiness (minimal compared to first-generation antihistamines)NauseaDyspepsia
Serious
  • Hypersensitivity reactions (anaphylaxis, angioedema, bronchospasm — rare)
  • QT prolongation (extremely rare; fexofenadine does NOT have the cardiotoxicity of its parent terfenadine)

Pregnancy & lactation

Pregnancy

FDA PLLR: Animal studies showed no teratogenicity at doses up to 3x MRHD. Limited human data. Generally considered safe in pregnancy. Recommended as first-line antihistamine in pregnancy by ACOG.

Lactation

Excreted in breast milk in very low concentrations. Minimal systemic exposure in nursing infant due to poor oral bioavailability. Compatible with breastfeeding per AAP.

Drug interactions

Aluminum Hydroxide
Moderate
Database

Decreased plasma concentrations of fexofenadine, potentially leading to reduced efficacy.

Administer fexofenadine at least 2 hours before or 2 hours after antacids containing aluminum or magnesium.

Source: DDInter

Amiodarone
Moderate
Database

Increased fexofenadine exposure, potentially leading to increased side effects.

Monitor for increased fexofenadine effects.

Antacids (aluminum And Magnesium Containing)
Moderate
Database

Reduced fexofenadine efficacy.

Separate administration by at least 2 hours.

Apalutamide
Moderate
Database

May result in decreased exposure to medications that are substrates of UGT, Pgp, BCRP, or OATP1B1 (e.g., fexofenadine, rosuvastatin).

Monitor for reduced efficacy of these medications. Dose adjustment or alternative agents may be necessary.

Source: DDInter

Cyclosporine
Moderate
Database

Increased fexofenadine exposure, potentially leading to increased side effects.

Monitor for increased fexofenadine effects.

Erythromycin
Moderate
Database

Erythromycin inhibits P-gp and OATP transporters, increasing fexofenadine plasma levels by 60-80%.

Monitor for increased antihistamine side effects. No dose adjustment typically needed but be aware of potential interaction.

Source: Kimi deep-research + Cla

Aluminum
Moderate
Database

Antacids containing aluminum and magnesium reduce fexofenadine absorption by binding/chelating the drug in the GI tract.

Separate administration by at least 2 hours. Give fexofenadine 2 hours before or after antacids.

Source: Kimi deep-research + Cla

Fruit Juices
Moderate
Database

Fruit juices inhibit intestinal OATP transporters (OATP1A2 and OATP2B1) that mediate fexofenadine absorption, reducing bioavailability by ~40%.

Take fexofenadine with WATER only. Avoid fruit juices within 4 hours of dosing. This is a critical counseling point.

Source: Kimi deep-research + Cla

Fruit Juices (grapefruit, Orange, Apple)
Moderate
Database

Decreased plasma concentrations of fexofenadine, potentially leading to reduced efficacy.

Advise patients to avoid taking fexofenadine with fruit juices. Take fexofenadine with water.

Ketoconazole
Moderate
Database

P-glycoprotein inhibitors increase fexofenadine plasma levels by blocking its efflux from intestinal enterocytes and renal tubular cells.

Monitor for increased side effects (headache, drowsiness). May need to reduce fexofenadine dose if used concurrently with strong P-gp inhibitors.

Source: Kimi deep-research + Cla

Magnesium Hydroxide
Moderate
Database

Decreased plasma concentrations of fexofenadine, potentially leading to reduced efficacy.

Administer fexofenadine at least 2 hours before or 2 hours after antacids containing aluminum or magnesium.

Source: DDInter

Rifampin
Moderate
Database

Rifampin induces P-glycoprotein, reducing fexofenadine absorption and plasma levels, potentially causing loss of efficacy.

Monitor for reduced antihistamine efficacy. May need to increase fexofenadine dose or switch to alternative antihistamine.

Source: Kimi deep-research + Cla

Related guidelines

Other Antihistamine drugs

Ask House about Fexofenadine

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Sources: KD Tripathi 7e, Goodman & Gilman 14e, Katzung, BNF·Verified: 2026-05-18 · House clinical team·Cockpit curated: 2026-05-18