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Zolase (Cetirizine)
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Zolase

Zolase is an antihistamine that reduces the natural chemical histamine in the body. Histamine can produce symptoms of sneezing, itching, watery eyes, and runny nose. It is used to treat cold or allergy symptoms such as sneezing, itching, watery eyes, or runny nose.

Other names for this medication:
Allerzine, Anncold, Cefid, Cepar, Cetariv, Cetmac, Cetnac, Cetracare, Cetricent, Cetriken, Cetrina, Cetrizine, Cezor, Combit, Decocet, Elart, Fomicet, Fulday, Gripcold, Histacid, Lecet, Lergi, Raincet, Reast, Relent, Sparzin, Sytra, Trucet

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Also known as: Cetirizine

Description

Zolase is developed by medical scientists to combat troublesome symptoms of outdoor and indoor allergy. Target of Zolase is to control, ward off, terminate and treat outdoor and indoor allergy. Zolase operates by making the level of natural chemical histamine lower to ward off outdoor (seasonal) and indoor allergy symptoms. Zolase is "non- sedating"antihistamine. Zolase is also known as Cetirizine, Reactine, Alercet, Alergex, Alerid, Certex-24, Cetrine, Cetzine, Cezin, Histazine, Riztec, Ryzen, Triz, Virlix, Xero-sed, Zirtin, Zyrzine.

Dosage

This section provides information on the proper use of a number of products that contain ketotifen. It may not be specific to Zolase Itchy Eye. Please read with care.

Do not wear contact lenses if your eyes are red . Also, do not use this medicine to treat irritation related to contact lens use. If you wear contact lenses: Take out your contact lenses before using ketotifen eye drops. Wait at least 10 minutes after putting the eye drops in before putting the contact lenses back in.

To use the eye drops:

First, wash your hands. Tilt the head back and, pressing your finger gently on the skin just beneath the lower eyelid, pull the lower eyelid away from the eye to make a space. Drop the medicine into this space. Let go of the eyelid and gently close the eyes. Do not blink. Keep the eyes closed for 1 to 2 minutes to allow the medicine to be absorbed by the eye. If you think you did not get the drop of medicine into your eye properly, use another drop. To keep the medicine as germ-free as possible, do not touch the applicator tip to any surface (including the eye). Also, keep the container tightly closed.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For ophthalmic dosage form (eye drops): For prevention of itching of the eye due to allergic conjunctivitis (eye allergy): Adults and children 3 years of age and older—Use one drop in each affected eye every 8 to 12 hours. Children up to 3 years of age—Use and dose must be determined by your doctor.

Overdose

Seek emergency medical attention if you think you have used too much of Zolase-D.

Storage

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Zolase 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

If you are breastfeeding, the chance that problems might occur depends on the ingredients of the combination. For the individual ingredients of these combinations, the following apply:

Acetaminophen—Acetaminophen passes into the breast milk. However, it has not been reported to cause problems in nursing babies. Alcohol—Alcohol passes into the breast milk. However, the amount of alcohol in recommended doses of this medicine does not usually cause problems in nursing babies. Antihistamines—Small amounts of antihistamines pass into the breast milk. Antihistamine-containing medicine is not recommended for use while breastfeeding since most antihistamines are especially likely to cause side effects, such as unusual excitement or irritability, in the baby. Also, since antihistamines tend to decrease the secretions of the body, the flow of breast milk may be reduced in some patients. Caffeine—Small amounts of caffeine pass into the breast milk and may build up in the nursing baby. However, the amount of caffeine in recommended doses of this medicine does not usually cause problems in nursing babies. Codeine and other narcotic cough medicines (e.g., dihydrocodeine, hydrocodone, and hydromorphone)—Codeine is changed to morphine in the body. Some people change codeine to morphine more quickly than others. These individuals are called "ultra-rapid metabolizers of codeine". If a nursing mother is an ultra-rapid metabolizer of codeine, it could lead to a morphine overdose in the nursing baby and cause very serious side effects. A nursing mother should talk to her doctor if she has any questions about taking codeine or about how this medicine may affect her baby . Decongestants (e.g., ephedrine, phenylephrine, pseudoephedrine—Phenylephrine has not been reported to cause problems in nursing babies. Ephedrine and pseudoephedrine pass into the breast milk and may cause unwanted effects in nursing babies (especially newborn and premature babies). 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. Salicylates (e.g., aspirin)—Salicylates pass into the breast milk. Although salicylates have not been reported to cause problems in nursing babies, it is possible that problems may occur if large amounts are taken regularly.

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Five new naturally occurring abietane diterpenoids (1-5) along with three known diterpenoids (6-8) were isolated from an acetone-soluble extract of the roots of Clerodendrum bungei. The genetic correction of the mutagenic properties of fotrin by using the interferon inducer larifan in spontaneously metastasizing Lewis lung carcinoma. The nonclassical correlations between the measurement results violate a generalized Bell inequality for four qubits. 115 of them were purchasers of a PERS, presented a lower index of independence in daily activities, greater fall history and a tendency to live alone. Agreement is generally very good and comparable to mutual experimental discrepancies. Effect of monomer structure on the mechanical properties of light-cured composite resins. Afternoon baseline GH was significantly higher in the women than in the men, but it was not significantly different between the female or the male patients and their respective matched controls. Acute undifferentiated leukemia (stem cell acute leukemia) showing differentiation to Langerhans cell-like cells in lymph nodes. The monocortical window (MCW): a modified split-crest technique adopting ligature osteosynthesis. E-speed emulsion was less affected than D-speed by fixer chemistry, time and temperature.

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Need of treatment with hemodialysis and kidney transplantation in Norway. This article reviews the literature on accrual in oncology clinical trials to characterize the extent of the problem, identify reasons for low accrual, and suggest ways to promote accrual. The theory of cancer stem cells states that a subset of cancer cells within a tumor has the ability to self-renew and differentiate. Data spanning from July 2002 to June 2005 were extracted from a comprehensive assessment tool, the Minimum Data Set, for 38,591 beneficiaries of a federal health insurance programme covering older adults in the Midwestern region of the United States of America. A significantly decreased number of T-lymphocytes was found both in case of ulcer disease of the stomach and gastric carcinoma. Hypomorphic Asns mutant mice have structural brain abnormalities, including enlarged ventricles and reduced cortical thickness, and show deficits in learning and memory mimicking aspects of what kind of drug is norvasc the patient phenotype. Our results emphasize the fact that human nondisjunction is a multifactorial trait that must be dissected into its component parts to identify specific associated risk factors. The State-of-the-art technologies such as GOPubmed use simple keyword-based techniques for retrieving abstracts from the PubMed and linking them to the Gene Ontology (GO). Somatostatin-receptor scintigraphy in gastroenteropancreatic tumors. It was shown that the structure should be finished with a low-index layer having a thickness larger than a quarter-wave to increase reflectivity, whereas layers below may remain of quarter-wave optical thickness at normal incidence angle.

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Peripheral blood mononuclear cells were assayed by flow cytometry for the cell surface markers CD3, CD8 and CD4 and for the intracellular cytokines interleukin 2 (IL 2), tumor necrosis factor-alpha (TNF-alpha), interferon-gamma (IFN-gamma) and interleukin 4 (IL 4). Editorial comment on: Molecular mechanisms related to parturition-induced stress urinary incontinence. Major disturbances of consciousness at the time of onset of focal central nervous system lesion were never observed. We sought additional information from the authors of three trials. The author discusses different strategies of linkage analysis incorporating these endophenotypes, including quantitative trait loci (QTL) linkage analysis, clustering-derived subgroups, ordered subset analysis (OSA), and latent classes for linkage scan. After incubation, the colonies were counted, Gram-stained and identified by biochemical tests. In this paper, we present the current views of the pathophysiological mechanisms underlying FDEIAn within the context of exercise immunology.

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Some of those alterations, such as c-abl rearrangements in certain leukemias, are characteristic of a certain type of malignancy. Although thyroid metabolism was apparently disregarded, the interference of microbiota on peripheral iodothyronine homeostasis is an intriguing issue. To determine whether the concentration of lead in bone constitutes a biological marker that is more sensitive for chronic toxicity than blood lead levels. This result was unexpected since the MDs typically contain very low levels of biologically active PAHs. In lichen planus and chronic eczema the dermis appeared as sound shadow.

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In reptiles there have been few studies examining the relationship between dopaminergic receptors and is prilosec an over the counter medication social behaviors. We have recently found a selective expansion of B1b cells concurrent with the resolution of B. In addition, peritoneal exudate cells from inoculated mice were capable of adoptively transferring immunity. We report here a patient treated with IL-2 and beta-IFN who rapidly developed an immune-mediated, bullous exfoliative dermatitis and who ultimately died. Intracellular desmocollin 3 and desmoglein 2 expression was observed by flow cytometry and cytoplasmic plakophilin 2 by immunofluorescence in all three MSC sources. Organophosphate-induced delayed polyneuropathy (OPIDP) is thought to be initiated by a variety of neuropathy target esterase (NTE) inhibitors. This analysis also reveals the cause of the dominance hierarchy at the protan and deutan loci, the perceptual effects of dosage compensation, and the phenotypes of various compound hemizygotes.

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