Article Contents ::
- 1 Details About Generic Salt :: Cetirizi
- 2 Main Medicine Class:: Antihistamine
- 3 (seh-TEER-ih-zeen) Zyrtec Class: Antihistamine
- 4 Drugs Class ::
- 5 Disclaimer ::
- 6 The Information available on this site is for only Informational Purpose , before any use of this information please consult your Doctor .Price of the drugs indicated above may not match to real price due to many possible reasons may , including local taxes etc.. These are only approximate indicative prices of the drug.
Details About Generic Salt :: Cetirizi
Main Medicine Class:: Antihistamine
(seh-TEER-ih-zeen)
Zyrtec
Class: Antihistamine
Drugs Class ::
Action Competitively antagonizes histamine at the H1 receptor site.
Indications for Drugs ::
Indications Symptomatic relief of symptoms (nasal and nonnasal) associated with seasonal and perennial allergic rhinitis; treatment of uncomplicated skin manifestations of chronic idiopathic urticaria.
Drug Dose ::
Route/Dosage
ADULTS & CHILDREN ³ 6 YR: PO 5 or 10 mg daily.
Hepatic Impairment: PO 5 mg daily.
Renal Impairment
CrU (31 ml/min or hemodialysis): PO 5 mg daily.
Contraindication ::
Contraindications Standard considerations.
Drug Precautions ::
Precautions
Pregnancy: Category B. Lactation: Excreted in breast milk. Children (< 6 yr): Safety and efficacy not established. Elderly patients: Side effect profile similar to younger patients. Renal and hepatic impairment: Dosage adjustment may be needed.
PATIENT CARE CONSIDERATIONS |
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Drug Side Effects ::
Adverse Reactions
CV: Palpitations; tachycardia; hypertension; cardiac failure; syncope. CNS: Somnolence; fatigue; dizziness; headache; paresthesia; confusion; hyperkinesia; hypertonia; migraine; tremor; vertigo; ataxia; dystonia; abnormal coordination, hyperesthesia; hypoesthesia, myelitis; paralysis; twitching; insomnia; sleep disorder; nervousness; depression; emotional lability; impaired concentration; anxiety; depersonalization; paranoia; abnormal thinking; agitation; amnesia; decreased libido; euphoria. DERM: Pruritus; dry skin; urticaria; acne; dermatitis; erythematous rash; increased sweating; alopecia; angioedema; furunculosis; bullous eruption; eczema; hyperkeratosis; hypertrichosis; photosensitivity; maculopapular rash; seborrhea; purpura; skin disorder; skin nodule. EENT: Pharyngitis; visual field defect; earache; blindness; loss of accommodation; eye pain; conjunctivitis; xerophthalmia; glaucoma; ocular hemorrhage; earache; tinnitus; deafness; sinusitis; nasal polyp; parosmia. GI: Dry mouth; nausea; vomiting; abdominal pain; diarrhea; anorexia; salivation; increased appetite; dyspepsia; flatulence; constipation; stomatitis; ulcerative stomatitis; aggravated tooth caries; tongue discoloration; tongue edema; gastritis; rectal hemorrhage; hemorrhoids; melena, eructation; enlarged abdomen; taste pervision; taste loss. GU: Urinary retention; polyuria; cystitis; dysuria; urinary tract infection; hematuria; micturition frequency; urinary incontinence; dysmenorrhea; female breast pain; intermenstrual bleeding; leukorrhea; menorrhagia; vaginitis. HEPA: Abnormal hepatic function. META: Thirst; dehydration; diabetes mellitus, weight gain. RESP: Epistaxis; rhinitis; coughing; bronchospasm; dyspnea; upper respiratory tract infection; hyperventilation; increased sputum; pneumonia; respiratory disorder. OTHER: Flushing; myalgia; arthralgia; arthrosis; arthritis; muscle weakness; lymphadenopathy; back pain; malaise; fever; asthenia; edema; rigors; pain; chest pain; leg cramps; ptosis.
Drug Mode of Action ::
Action Competitively antagonizes histamine at the H1 receptor site.
Drug Interactions ::
Interactions None well documented.
Drug Assesment ::
Assessment/Interventions
- Obtain patient history, including drug history and any known allergies, especially to antihistamines.
- Assess for allergy symptoms (eg, rhinitis, conjunctivitis, hives) before and periodically throughout the therapy.
- Monitor pulse, blood pressure and respirations periodically throughout therapy.
- Observe for dizziness and excessive sedation.
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Drug Storage/Management ::
Administration/Storage
- Give as 2 single daily doses, without regard to meals.
- Available in PO tablets or liquid.
- Store tablets at room temperature (59°–86°F), liquid at 41°–86°F.
Drug Notes ::
Patient/Family Education
- Advise patient that drug may cause drowsiness and to use caution while driving or performing other tasks requiring alertness until response to medication is known.
- Advise patient that photosensitivity may occur and to take protective measures (eg, sunscreens, protective clothing) against exposure to ultraviolet light or sunlight until tolerance is determined.
- Caution patients to avoid using alcohol or other CNS depressants (eg, sedatives, hypnotics, tranquilizers).
- Instruct patient to take sips of water frequently, suck on ice chips or sugarless hard candy, or chew sugarless gum if dry mouth occurs.
- If patient is to have allergy skin testing, advise to avoid taking medication for at least 4 days before test.