Registered Kenya · PPB

ULTIGRA 120 TABLETS

FEXOFENIDINE HYDROCHLORIDE TABLETS USP 120 MG

What it does

Fexofenadine is an antihistamine that helps relieve allergy symptoms.

Commonly used for: seasonal allergies (hay fever), chronic hives (urticaria)

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
H2008/18195/085
Registration date
-
Expiry date
-
Status
Registered
Active ingredient
FEXOFENIDINE HYDROCHLORIDE TABLETS USP 120 MG
Strength
-
Pack size
-
Therapeutic class
-
Manufacturer / MAH
Zawadi Healthcare
Applicant / LTR
-
Country of origin
FOREIGN
Manufacturer location
Shop 2, Next To Gen. Shop, Near Deliverance Church, Off Depot Road, Nairobi, Kenya

Source: Pharmacy and Poisons Board · fetched 2026-01-28 21:29:24 · updated 2026-07-20 11:03:38

Disclaimer: This information is sourced from Pharmacy and Poisons Board (Kenya). Always consult a qualified healthcare professional before using any medication.

About this medicine

Fexofenadine is an antihistamine that helps relieve allergy symptoms.

What it treats

  • seasonal allergies (hay fever)
  • chronic hives (urticaria)

How it works

It blocks the action of histamine, a substance in the body that causes allergic symptoms.

Who it's for

Fexofenadine is suitable for adults and children with allergy symptoms.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: fexofenidine

Fexofenadine is a second-generation antihistamine used primarily for the relief of symptoms associated with allergic rhinitis and urticaria. It is less sedating than first-generation antihistamines due to its limited penetration across the blood-brain barrier, making it a preferred choice for patients who require allergy relief without the sedative effects.

Indications

  • Allergic rhinitis
  • Seasonal allergic rhinitis
  • Chronic idiopathic urticaria

Dosage

Children: Refer to the BNF for Children for specific dosing guidelines for paediatric patients.

Adults: Refer to the BNF for specific dosing guidelines for adults.

Mechanism of action

Fexofenadine works as a selective antagonist of peripheral H1 receptors, inhibiting the action of histamine, a substance in the body that causes allergic symptoms. By blocking these receptors, fexofenadine reduces the symptoms of allergies such as sneezing, itching, and runny nose.

Pharmacodynamics

Fexofenadine exhibits a rapid onset of action, typically effective within one hour of administration, and its effects can last for up to 24 hours. It does not significantly affect the central nervous system, which minimizes the risk of sedation. The drug is well-tolerated in most patients, with a side effect profile that includes headache, dizziness, and gastrointestinal disturbances.

Pharmacokinetics

Fexofenadine is absorbed in the gastrointestinal tract, with peak plasma concentrations occurring approximately 2 to 3 hours post-administration. It has a bioavailability of about 33% due to first-pass metabolism. The drug is largely excreted unchanged in the urine, with an elimination half-life of approximately 14.4 hours, allowing for once-daily dosing in most cases.

Adverse effects

  • Headache
  • Dizziness
  • Somnolence
  • Dry mouth
  • Nausea

Interactions

  • Antacids containing aluminum or magnesium may reduce the absorption of fexofenadine
  • Erythromycin and ketoconazole may increase plasma concentrations of fexofenadine

Precautions

  • Use with caution in patients with renal impairment
  • Caution should be exercised when driving or operating machinery until individual response to the medication is known

Pregnancy

Fexofenadine should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. Limited data available.

Breast-feeding

Fexofenadine is excreted in human milk, caution should be exercised when administering to nursing mothers.

Storage

Store in a cool, dry place away from direct sunlight. Keep out of reach of children.

Formulations

  • Tablets
  • Oral suspension

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.