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Allofex (Fexofenadine)

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Allofex 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. Allofex 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, Allegix, Altiva, Evafex, Fegix, Fenofex, Fexigra, Fexise, Fexodin, Fexodis, Fexody, Fexofast, Fexofen, Fexohist, Fexokast, Fexolast, Fexona, Fexopark, Fexopride, Fexoquin, Fexoquit, Fexor, Fexoriv, Fexot, Fexotab, Fexotive, Fexova, Fexozide, Fextral, Histakind, Histaloc, Irmont, Maxgra, Montair, Montemac, Monten, Novamont, Odifex, Ofena, Oregra, Radifex, Rhinofex, Ultigra, Xdine, Zegra

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Also known as: Fexofenadine


Allofex is produced by Sanofi Aventis. The raw material is Fexofenadine that is an antihistamine with selective peripheral H1-receptor antagonist activity.


This section provides information on the proper use of a number of products that contain fexofenadine. It may not be specific to Allofex ODT. Please read with care.

You should always take this medicine with water. Do not take it with juice such as grapefruit, orange, or apple juice .

You should NOT take antacids that contain aluminum or magnesium hydroxide within 15 minutes of taking this medicine. If you are uncertain about this, ask your doctor or pharmacist .

For patients using the oral disintegrating tablet form of this medicine:

Make sure your hands are dry. Do not push the tablet through the foil backing of the package. Instead, gently peel back the foil backing and remove the tablet. Immediately place the tablet on top of the tongue. Do not chew or break the tablet. The tablet will dissolve in seconds, and you may swallow it with your saliva. You may drink a glass of water after the tablet has dissolved. Always take this tablet on an empty stomach .

Shake the oral liquid well before using it. Measure the liquid with a marked measuring spoon, oral syringe, or medicine cup .

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 symptoms of hay fever: For oral dosage form (capsules, tablets): Adults and children 12 years of age and older—60 milligrams (mg) two times a day, or 180 mg once a day. Children 6 to 11 years of age—30 mg two times a day. Children 4 to 6 years of age—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 (disintegrating tablets): Children 6 to 11 years of age—30 milligrams (mg) two times a day, on an empty stomach. Children 4 to 6 years of age—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 (suspension): Children 4 to 11 years of age—30 milligrams (mg) or 5 milliliters (mL) two times a day. Children younger than 4 years of age—Use and dose must be determined by your doctor .

For symptoms of chronic hives: For oral dosage form (capsules, tablets): Adults and children 12 years of age and older—60 milligrams (mg) two times a day, or 180 mg once a day. Children 4 to 11 years of age—30 mg two times a day. Children younger than 4 years of age—Use and dose must be determined by your doctor . For oral dosage form (disintegrating tablets): Children 4 to 11 years of age—30 milligrams (mg) two times a day, on an empty stomach. Children younger than 4 years of age—Use and dose must be determined by your doctor . For oral dosage form (suspension): Children 4 to 11 years of age—30 milligrams (mg) or 5 milliliters (mL) two times a day. Children 6 months to 4 years of age—15 mg or 2.5 mL two times a day. Children younger than 6 months of age—Use and dose must be determined by your doctor .


If an overdose occurs and you are not feeling well, stop taking the medication immediately. You should seek emergency medical attention or contact your healthcare 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 Allofex ODT dosage information

Side effects

The most common side effects associated with Allofex 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.


You should not use Children's Allofex Allergy if you are allergic to it.

Ask a doctor or pharmacist if Children's Allofex Allergy is safe to use if you have:

kidney disease.

Ask a doctor before using this medicine if you are pregnant or breastfeeding.

Older adults may be more sensitive to the effects of this medicine. If you are 65 or older, ask a doctor before taking Children's Allofex Allergy.

This medicine may contain phenylalanine. Tell your doctor if you have phenylketonuria (PKU).

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When heat-killed Propionibacterium acnes is intravenously injected into rats followed by an intravenous injection of a small amount of Gram-negative lipopolysaccharide (LPS) 7 days later, massive hepatic cell necrosis is induced and most of the rats die within 24 hours of LPS injection. pyogenes from phagocytosis at the site of initial infection, allowing it to invade host tissues during severe infections. Sixteen temporomandibular joints from 15 patients, reported to have disc perforation at arthrography, were studied. The mechanism of cell death was studied in taxane-resistant ovarian cancer cells and in tumor sections obtained from different mouse tumors. LDI represents an accurate and fast dose calculation algorithm for treatment planning. These findings describe the mechanisms by which JUN influences PRKCC signaling and provide additional and novel insight into the regulation of the steroidogenic machinery in mouse Leydig cells. This study investigated whether AP could improve established prostate hyperplasia using the same testosterone propionate (TP)-induced prostate hyperplasia model in rats. Further investigation is needed to determine optimal dosing and route of delivery. Chagas disease is characterized by cardiac lesions and a high level of PGE2. These results are consistent with the structure changes of the vortex lattice in CeCoIn5 in H parallel c determined from recent neutron scattering data.

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Items from Medical Outcomes Study Short Form-36 were used to measure pain intensity and pain interference in daily life. The fistula was occluded percutaneously, which allowed the patient to stabilise haemodynamically and, finally, to undergo a definitive surgical excision of the pseudoaneurysm and repair of the sporanox aortic defect. Quantization of a free particle interacting linearly with a harmonic oscillator. The results showed that HT reduced the AA-induced genotoxicity by decreasing the ROS level and increasing the GSH level. Laparoscopic liver resection is a procedure of significant risk and is more technically demanding in comparison with traditional open method. The results obtained in this study partially explain why hydrophilic NOM dominated over humic substances in foulants of membranes used for water treatment in recent studies on fouling. Endoscopic ultrasonography (EUS) identified a 6- to 7-mm tumor at the juncture of the head and body of the pancreas. On each study day, lower body skin temperature was maintained near 38 degrees C and upper body skin temperature near 33 degrees C.

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The rectifying of infertility by application of modern technology has been a topic for debate in modern society over the past decade. The two-factorial symptom structure of post-traumatic stress disorder: depression-avoidance and arousal-anxiety. In vivo study of chitosan-natural nano hydroxyapatite scaffolds for bone tissue regeneration. Role of receptor polymorphism and glycosylation in syncytium induction and host range variation of ecotropic mouse gammaretroviruses. Lack of association between LOXL1 gene polymorphisms and primary open angle glaucoma in the Saudi Arabian population. 2) Pitch percepts in response to electric stimulation may be modified by experience. Experiments using synthetic and clinical data show that the proposed method reduces intensity variability in tissues and improves the distinction between key tissue types.

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