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Zyrtec 10 mg. Ded irritability fussiness, insomnia, fatigue, and malaise. ZYRTEC-D 12 HOUR® (cetirizine HCl 5 mg pseudoephedrine HCl 120 mg) Extended Release Tablets In ZYRTEC studies, side effects were mild or moderate, including drowsiness, fatigue, and dry mouth in adults, and drowsiness, headache, sore throat, and stomach pain in children. Drowsiness occurred in between 11% and 14% in adults, depending on dose, compared with 6% taking placebo. In children, drowsiness occurred in between 2% and 4%, depending on dose, compared with 1% taking placebo. Due to its pseudoephedrine component, ZYRTEC-D 12 HOUR is contraindicated in patients with narrow-angle glaucoma, urinary retention, severe hypertension, or severe coronary artery disease, and in patients receiving monoamine oxidase (MAO) inhibitor therapy, or within fourteen (14) days of stopping such treatment. It should also be used with caution in patients with hypertension, diabetes mellitus, ischemic heart disease, increased intraocular pres zyrtec 10

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Sure, hyperthyroidism, renal impairment, or prostatic hypertrophy. Pseudoephedrine hydrochloride may produce arrhythmias and cardiovascular collapse with accompanying hypotension. Care should be taken in the concomitant administration of other sympathomimetic amines because combined effects on the cardiovascular system may be harmful to the patient. Pseudoephedrine hydrochloride may cause CNS stimulation in hypersensitive patients. Nervousness, excitability, convulsions, tremor, restlessness, dizziness, weakness, or insomnia may occur. The elderly are more likely to experience adverse reactions to sympathomimetic amines. ZYRTEC is available in 5 mg and 10 mg tablets, 5 mg and 10 mg chewable tablets, and 1 mg mL syrup. ZYRTEC-D 12 HOUR is available in an extended release tablet. The health information contained herein is provided for educational purposes only and is not intended to replace discussions with a healthcare provider. All decisions regarding patient care must be made with a h zyrtec 10

zyrtec 10 mg:

zyrtec 10 mg Though no clinically significant drug interaction was seen with a low dose of theophylline (a drug used for asthma zyrtec 10 mg, chronic bronchitis zyrtec 10 mg, emphysema zyrtec 10 mg, or chronic obstructive pulmonary disease) zyrtec 10 mg, a 400 mg dose of theophylline caused a slightly prolonged presence of cetirizine in the blood. It is possible that larger theophylline doses could have a greater effect. If you have any questions or concerns zyrtec 10 mg, be sure to consult your doctor. For full prescribing information zyrtec 10 mg, click here. ZYRTEC-D 12 HOUR® Extended Release Tablets ZYRTEC-D 12 HOUR® Extended Release Tablets contain 5 mg of cetirizine HCl for immediate release and 120 mg of pseudoephedrine HCl for exte zyrtec 10 mg.

zyrtec 10 mg Nded release in a bilayered tablet. ZYRTEC-D 12 HOUR® Extended Release Tablets can be taken with or without food zyrtec 10 mg, and should be swallowed whole (not broken or chewed). Be sure to take ZYRTEC-D 12 HOUR® Extended Release Tablets exactly as prescribed by your doctor. Adults and children 12 years or older: The recommended dose of ZYRTEC-D 12 HOUR® Extended Release Tablets is one tablet twice a day. Taking ZYRTEC-D 12 HOUR® Extended Release Tablets with other medications and medical conditions: Due to the pseudoephedrine component zyrtec 10 mg, you should not take ZYRTEC-D 12 HOUR® Extended Release Tablets if you have taken monoamine oxidase (MAO) inhibitors in the past 14 days. Taking ZYRTEC-D 12 HOUR® Extended Release Tablets with some blood pressure medications may reduce their effectiveness on blood pressure control). Disturbances on how your heart beats can occur when pseudoephedrine is used with digitalis. Care should be taken when ZYRTEC-D 12 HOUR® Extended Release Tablets are taken with other sympathomimetic amines (for example zyrtec 10 mg, some inhaled medications for the treatment of asthma) because combined effects on the cardiovascular system may be harmful to the patient. Inform your doctor if you have or have ever had high blood pressure zyrtec 10 mg, heart disease zyrtec 10 mg, glaucoma zyrtec 10 mg, diabetes zyrtec 10 mg, an overactive thyroid gland.

zyrtec 10 mg S in the past 14 days. Taking ZYRTEC-D 12 HOUR® Extended Release Tablets with some blood pressure medications may reduce their effectiveness on blood pressure control). Disturbances on how your heart beats can occur when pseudoephedrine is used with digitalis. Care should be taken when ZYRTEC-D 12 HOUR® Extended Release Tablets are taken with other sympathomimetic amines (for example zyrtec 10 mg, some inhaled medications for the treatment of asthma) because combined effects on the cardiovascular system may be harmful to the patient. Inform your doctor if you have or have ever had high blood pressure zyrtec 10 mg, heart disease zyrtec 10 mg, glaucoma zyrtec 10 mg, diabetes zyrtec 10 mg, an overactive thyroid gland zyrtec 10 mg, .

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Ch as histamine, together with a selective action on the H1 receptors. Cetirizine reduces eosinophil recruitment induced by an antigen-antibody reaction. PHARMACOKINETIC PROPERTIES: Peak blood levels of 300 ng mL are reached within one hour after oral administration of cetirizine. Cetirizine does not undergo extensive first pass metabolism. The terminal half life is approximately 10 hours in adults, 6 hours in children aged 6 to 12 years and 5 hours in children aged 2 to 6 years. These data are consistent with the urinary excretion half-life of the drug. The cumulative urinary excretion represents about two thirds of the dose given in both adults and children. The apparent plasma clearance in children is higher than that measured in adults. Plasma levels are linearly related to the dosage given. A high proportion of cetirizine is bound to human plasma proteins. In patients with impaired renal clearance (less than 40 mL min) and hepatic insufficiency, an increase in half-life and decrease in total creatinine clearance occurs. INDICATIONS: Allergic processes responding to a histamine H1 receptor antagonist. & 150; Respiratory: Allergic rhinitis, hay fever. & 150; Cutaneous: Allergic skin conditions associated with pruritus e.g. urticaria. CONTRA-INDICATIONS: History of hypersensitivity to any of the constituents of the formulations. Hypersensitivity to hydroxyzine. ZYRTEC® is contra-indicated in lactating women since the active ingredient is excreted in breast milk. ZYRTEC® is contra-indicated in pregnancy as the safety has not been established. DOSAGE AND DIRECTIONS

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