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Alzine (Cetirizine)
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Alzine

Alzine is an antihistaminic medication. It treats allergy symptoms such as itching, swelling, and rashes by blocking the effects of a chemical messenger (histamine) in the body. This medicine is generally very safe. The most common side effects include feeling sleepy or dizzy.

Other names for this medication:
Alerbloc, Algine, Cetafed, Cetaz, Cetchem, Cetcip, Ceter, Cetikin, Cetiminic, Cetiz, Cetram, Cetrich, Cetrimin, Cetrish, Cetup, Cetven, Cetzikan, Citol, Cofstop, Coldar, Eltrazin, Excet, Flomicet, Fluban, Histanit, Kidcet, Kofrid, Lacold, Lexicet, Okacet, Parcet, Quzine, Sizon, Solodryl, Sparcet, Zucet

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Also known as: Cetirizine

Description

{name} (cetirizine) is an antihistamine that reduces the effects of natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose.

{name} is used in adults and children to treat cold or allergy symptoms such as sneezing, itching, watery eyes, or runny nose.

{name} is also used to treat itching and swelling caused by chronic urticaria (hives).

Dosage

Usual Adult Dose for Allergic Rhinitis:

5 to 10 mg orally once a day -Maximum dose: 10 mg/day -Some experts recommend: Patients over 65 years of age should start with 5 mg orally once a day.

Usual Adult Dose for Urticaria:

5 to 10 mg orally once a day -Maximum dose: 10 mg/day -Some experts recommend: Patients over 65 years of age should start with 5 mg orally once a day. Uses: -Relief of symptoms associated with perennial allergic rhinitis due to allergens (e.g., sneezing, rhinorrhea, postnasal discharge, nasal pruritus, ocular pruritus, tearing) -Treatment of uncomplicated skin manifestations of chronic idiopathic urticaria

Usual Pediatric Dose for Allergic Rhinitis:

6 months to 2 years: -Initial dose: 2.5 mg orally once a day -Maintenance dose: 2.5 mg orally once to 2 times a day -Maximum dose: 5 mg/day 2 to 5 years: -Initial dose: 2.5 mg orally once a day -Maintenance dose: 2.5 mg orally 2 times a day OR 5 mg orally once a day -Maximum dose: 5 mg/day 6 years and older: 5 to 10 mg orally once a day -Maximum dose: 10 mg/day

Usual Pediatric Dose for Urticaria:

6 months to 2 years: -Initial dose: 2.5 mg orally once a day -Maintenance dose: 2.5 mg orally once to 2 times a day -Maximum dose: 5 mg/day 2 to 5 years: -Initial dose: 2.5 mg orally once a day -Maintenance dose: 2.5 mg orally 2 times a day OR 5 mg orally once a day -Maximum dose: 5 mg/day 6 years and older: 5 to 10 mg orally once a day -Maximum dose: 10 mg/day Uses: -Relief of symptoms associated with perennial allergic rhinitis due to allergens (e.g., sneezing, rhinorrhea, postnasal discharge, nasal pruritus, ocular pruritus, tearing) in patients 2 years and older -Treatment of uncomplicated skin manifestations of chronic idiopathic urticaria in patients 6 months and older

Detailed Alzine dosage information

Overdose

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

Overdose symptoms may include extreme drowsiness, vision problems, agitation, feeling restless and then drowsy or tired, fast heartbeats, stomach pain, nausea, vomiting, trouble walking, or trouble swallowing or speaking.

Storage

Keep out of the reach of children.

Store the medicine in a closed container at room temperature, away from heat, moisture, and direct light. Keep from freezing.

Do not keep outdated medicine or medicine no longer needed.

Keep the liquid form of this medicine from freezing. Do not refrigerate the syrup.

Side effects

The most common side effects associated with Alzine are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

Very young children are usually more sensitive to the effects of this medicine. Before giving any of these combination medicines to a child, check the package label very carefully. Some of these medicines are too strong for use in children. If you are not certain whether a specific product can be given to a child, or if you have any questions about the amount to give, check with your health care professional, especially if it contains:

Antihistamines—Nightmares, unusual excitement, nervousness, restlessness, or irritability may be more likely to occur in children taking antihistamines. Decongestants (e.g., ephedrine, phenylephrine, pseudoephedrine—Increases in blood pressure may be more likely to occur in children taking decongestants. Iodides (e.g., calcium iodide and iodinated glycerol)—These medicines pass into the breast milk and may cause unwanted effects, such as underactive thyroid, in the baby. Narcotic antitussives (e.g., codeine, dihydrocodeine, hydrocodone, and hydromorphone)—Breathing problems may be especially likely to occur in children younger than 2 years of age taking narcotic antitussives. Also, unusual excitement or restlessness may be more likely to occur in children receiving these medicines. Salicylates (e.g., aspirin)—Do not give medicines containing aspirin or other salicylates to a child or teenager with a fever or other symptoms of a virus infection, especially flu or chickenpox, without first discussing its use with your child's doctor. This is very important because salicylates may cause a serious illness called Reye's syndrome in children with fever caused by a virus infection, especially flu or chickenpox. Also, children may be more sensitive to the aspirin or other salicylates contained in some of these medicines, especially if they have a fever or have lost large amounts of body fluid because of vomiting, diarrhea, or sweating.

Do not give any over-the-counter (OTC) cough and cold medicine to a baby or child under 4 years of age. Using these medicines in very young children might cause serious or possibly life-threatening side effects .

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Establishing cleft malformation surgery in developing nations: a model for the new millennium. Whereas most cases exhibited cytoplasmic or cytoplasmic and nuclear PIM1 and PIM2 expression, 12 cases (10 of the non-germinal centre DLBCL type) expressed PIM1 predominately in the nucleus. Malaria episode data for Kahnooj District, south-east Iran, were collected from the local health system for the period 1994-2002. The liner correlation analysis was carried out between the mean optical densities and CT values for the four areas of interest. At the end of the swim trial, the maturation parameters 11-ketotestosterone, pituitary levels of LH and plasma levels of estradiol were higher (although not significantly) in the Swim compared to the End Control group. Male Wistar rats were treated (1 or 21 d, i.p.) with fluoxetine, buspirone or vehicle, once daily. Under these conditions, the plasma fibrinogen levels peaked by 24 h in young animals, being up to 7-fold over the values of untreated controls at 72 h. As a result, KCTD2 depletion acquires GSC features and affects aerobic glycolysis via expression changes in glycolysis-associated genes through c-Myc protein regulation. A computational model is potentially a powerful tool to apprehend complex phenomena like solid tumour growth and to predict the outcome of therapies. Rats received vehicle, aripiprazole (2, 5, or 15 mg/kg), or cariprazine (0.06, 0.2, or 0.6 mg/kg) for 28 days.

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The L2-4,6 and L5 cells located in the left upper quadrant of the abdominal ganglion of Aplysia californica express the L5-67 and LUQ-1 genes, respectively, in a nonoverlapping manner. It was shown that FGF2 induces the proliferation of pancreatic epithelial cells during embryonic life. Results on the ventricles and on the heart muscle are presented and compared with manually segmented models. Non-linear summation of AMPA-mediated PSPs was measured experimentally when two monosynaptic pathways to motoneurones were stimulated. This is a promising new method to circumvent some of the difficulties associated with closure of large ASDs and deficient aortic rim. Substantial overexpression of cathepsin D was found in the poorly differentiated tumors. Therefore, systemic radionuclide therapy must be considered as a valuable and effective method of treatment in patients with widespread skeletal metastases. These results suggest that OBCAM is responsible for controlling the cell proliferation and growth in cortical astrocytes. Increased mutant frequency and altered mutation spectrum of the lacI transgene in Wilson disease rats with hepatitis.

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In contrast to earlier reports, we could not demonstrate a risk-modifying effect of genetic polymorphisms in mEH on head and neck carcinogenesis, except for the predicted high activity variant in patients with hypopharyngeal carcinoma. The patient presented with seizures and a reduced level of consciousness. Well designed interventional human studies of the upper airway, which account for complex gene-environment-diet interactions, will be necessary to adequately examine the potential clinical benefit of antioxidant therapies for rhinosinusitis. Here we report that the cytoplasmic domain of beta1-integrin specifically interacts with the cytoskeletal protein filamin. These results encourage the use of such deformation based expression quantification measures for research in clinical applications that require the automated measurement of facial affect. We show working memory effects during the retention period in early visual cortex which were retinotopically organized in the sense that evoked BOLD responses were specific to the position of the remembered location on an imaginary clock. The mechanism bears analogy to interface dynamics in condensed media.

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