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Altiva (Fexofenadine)

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Altiva is an effective medical drug for allergy caused by chemical histamine which is formed in our body naturally and reacts to the external irritants causing the allergic reaction. Altiva blocks the production and increased activity of histamine receptors as a result of which there is a reduction of the response reaction to the external irritants and the main symptoms of allergy are reduced. This drug helps to reduce cold, lacrimation, sneezing, itching, edema and other allergic symptoms.

Other names for this medication:
Afexdine, Alafex, Allefast, Allegix, Allofex, Ancofex, Coligra, Evafex, Exfen, Faydine, Fegix, Fegra, Fenadin, Fendosh, Fenixa, Ferodra, Fexamin, Fexigra, Fexise, Fexocare, Fexodin, Fexodine, Fexody, Fexofen, Fexofenadine, Fexohist, Fexopark, Fexoquin, Fexoquit, Fexor, Fexoriv, Fexot, Fexova, Fexozide, Histakind, Histaloc, Infexo, Irmont, Jorifex, Madexa, Maxgra, Montair, Montemac, Monten, Nexofex, Ofena, Oregra, Radifex, Xdine, Zegra

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Also known as: Fexofenadine


Generic Altiva is developed by medical scientists to combat troublesome symptoms of outdoor allergy. Target of Generic Altiva is to control, ward off, terminate outdoor allergy. Generic Altiva acts as an anti-allergy remedy. Generic Altiva operates by making the level of natural chemical histamine lower to ward off outdoor (seasonal) allergy symptoms. Generic Altiva is antihistamine. Generic name of Generic Altiva is Fexofenadine. Altiva is also known as Fexofenadine, Telfast, Fastofen, Fexo-120, Fexigra. Brand names of Generic Altiva are Altiva, Altiva-D 12 Hour, Altiva Oral Suspension, Altiva-D 24 Hour.


This section provides information on the proper use of a number of products that contain fexofenadine and pseudoephedrine. It may not be specific to Altiva-D. Please read with care.

Swallow the extended-release tablet whole. Do not crush, break, or chew it before swallowing.

This medicine is best taken on an empty stomach (either one hour before or two hours after a meal).

This medicine should be taken with water. Do not take with fruit juices or antacids.

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 oral dosage form (extended-release tablets [12 hour]): For symptoms of hay fever: Adults and teenagers—1 tablet two times a day. Children 4 years of age and older—Use and dose must be determined by your doctor. Children and infants up to 4 years of age—Use is not recommended . For oral dosage form (extended-release tablets [24 hour]): For symptoms of hay fever: Adults and teenagers—1 tablet one time a day. Children 4 years of age and older—Use and dose must be determined by your doctor. Children and infants up to 4 years of age—Use is not recommended .


If you overdose Generic Altiva and you don't feel good you should visit your doctor or health care provider immediately.


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

Keep out of the reach of children.

Do not keep outdated medicine or medicine no longer needed.

Ask your healthcare professional how you should dispose of any medicine you do not use.

Detailed Altiva ODT dosage information

Side effects

The most common side effects associated with Altiva 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.


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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Validation of the smoking habits of a sample of the patient population seen in a pulmonary function laboratory. A pilot-scale soil washing process, patented by BioTrol, Inc., was demonstrated on soil contaminated by wood treating waste, primarily pentachlorophenol (PCP) and creosote-derived polynuclear aromatic hydrocarbons (PAHs). Scutisorex, the hero shrew, is an East African species of shrew with what is likely the most highly modified vertebral morphology in the entire history of mammals. According to current views, the parietal cortex produces attentional signals that filter out irrelevant information in the ventral visual stream. When applied phenotypically, selection on predicted lean tissue growth rate will result in selection differentials for both fat and lean tissue growth rates that are proportional to those obtained by direct selection for lean tissue growth rate. Six of the specimens, from north of Tucson, produced venom lethal toxicity (i.p.

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Melanocyte stimulating hormone and the inhibition of sexual behaviour in the female rat. Pleiotropic effects of ribosomal mutations for cycloheximide resistance in a double-resistant homocaryon of Neurospora crassa. This system, for the first time, clearly relates an in vivo symptom and mediator release and thus should provide an excellent tool for the further study of the allergic response and nasal pathophysiology. 2: Relationship of Aedes taeniorhynchus eggshell density to larval albenza annual cost production. In the case of mouse, juvenile flukes penetrated the duodenum, jejunum, cecum, and rectum at considerably high rates. Periodicity in protein metabolism: time patterns of substrate interaction and utilization. In the lamina epithelialis mucosae of human duodenal biopsies 5-hydroxytryptamine in enteroendocrine EC cells was demonstrated by means paraformaldehyde induced fluorescence and impregnation techniques. To our knowledge, this is the first published case that describes the association between a low-dose fluoxetine regimen and the evolution of a bipolar affective state from depression to euthymia via manic switching. Two statistical effect size measures to contend with attrition (dropout d and total attrition d) are offered for future researchers and policy makers. However, in symptomatic older patients whose hydronephrosis was not first identified on prenatal sonography, a vessel was the cause of obstruction in one half.

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