Clarinex Reditabs Side Effects

Generic Name: desloratadine

Please note - some side effects for Clarinex Reditabs may not be reported. Always consult your doctor or healthcare specialist for medical advice. You may also report side effects to the FDA.

Side Effects of Clarinex Reditabs - for the Consumer

Clarinex Reditabs Orally Disintegrating Tablets

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome when using Clarinex Reditabs Orally Disintegrating Tablets:

Dizziness; drowsiness; dry mouth; menstrual pain; muscle pain; nausea; sore throat; tiredness; upset stomach.

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, throat, or tongue); dark urine; fast or irregular heartbeat; pale stools; seizures; yellowing of the skin or eyes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.

Side Effects by Body System - for Healthcare Professionals

Cardiovascular

Cardiovascular side effects of spontaneous nature reported during the marketing of desloratadine have included tachycardia and palpitations.

Hypersensitivity

Hypersensitivity side effects of spontaneous nature reported during the marketing of desloratadine have included rash, pruritus, urticaria, edema, dyspnea, and anaphylaxis.

Hepatic

Hepatic side effects have included elevated liver enzymes and bilirubin. Very rarely, hepatitis has been observed in clinical practice.

Gastrointestinal

Gastrointestinal side effects have included dry mouth, dry throat, nausea, and pharyngitis.

Nervous system

Nervous system side effects have included somnolence and dizziness. Psychomotor hyperactivity and seizures have been observed in clinical practice.

An increase in the incidence of somnolence has been reported in clinical trials (n=1838) at doses of 10 mg/day and 20 mg/day (5.2% and 7.6%, respectively), compared to placebo (2.3%).

General

General side effects have included myalgia and influenza-like symptoms.

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