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Alfexo (Fexofenadine)

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Alfexo is used for treating seasonal allergy symptoms such as sneezing, runny nose, itchy throat, or itchy, watery eyes, skin itching and hives caused by a condition called chronic idiopathic urticaria.

Other names for this medication:
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Also known as: Fexofenadine


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


Use Alfexo exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended.

Take the regular tablet with a full glass of water. Do not use any other type of liquid. Shake the oral suspension (liquid) well just before you measure a dose. To be sure you get the correct dose, measure the liquid with a marked measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

To take fexofenadine orally disintegrating tablets (Alfexo ODT):

Keep the tablet in its blister pack until you are ready to take the medicine. Open the package and peel back the foil from the tablet blister. Do not push a tablet through the foil or you may damage the tablet. Using dry hands, remove the tablet and place it in your mouth. It will begin to dissolve right away. Do not swallow the tablet whole. Allow it to dissolve in your mouth without chewing. Swallow several times as the tablet dissolves. If desired, you may drink liquid to help swallow the dissolved tablet.

Take the Alfexo disintegrating tablet on an empty stomach, at least 1 hour before or 2 hours after a meal.

Tell your doctor if your symptoms do not improve, or if they get worse after you start taking Alfexo. Never use more than the recommended dose.

Store Alfexo at room temperature away from moisture and heat. Keep the medicine bottle tightly closed.

Detailed Alfexo dosage information


If you overdose Generic Alfexo 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Do not keep outdated medicine or medicine no longer needed.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 Alfexo ODT dosage information

Side effects

The most common side effects associated with Alfexo 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.


Use is not recommended in infants and children up to 12 years of age. In children 12 years of age and older, this medicine is not expected to cause different side effects or problems than it does in adults.

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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Reconstruction of a severe chest and abdominal wall electrical burn injury in a pediatric patient. Tissue-specific transgene expression in the prostate epithelium has previously been achieved using short prostate-specific promoters, rendering transgenic mouse lines susceptible to integration site-dependent effects. Complementary DNA (cDNA) was reverse transcribed from the mRNAs and used as a probe for fluorescent in situ hybridization to metaphase chromosomes. Effects of Dexamethasone in the Treatment of Recurrent Chronic Subdural Hematoma. The inclusion complexation behavior between 10-undecyn-1-ol and cyclodextrin (CD) derivatives, namely, randomly methylated beta-CD (RM-beta-CD) and hydroxypropyl-beta-CD (HP-beta-CD), was studied in terms of solubility improvement, apparent stability constant, and the inclusion ratios of the resultant inclusion complexes. The effects of continuous ambulatory peritoneal dialysis (CAPD) on serum lipids and lipoproteins over the initial year of therapy were studied in 23 uremic patients. The typical effective dose was 7.5 mSv for male patients and 10.2 mSv for female patients. All these features might result in improved target-organ damage. Oyster Shell Protein and Atomic Force Microscopy of Oyster Shell Folia.

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We have examined the effects of curcumin on a panel of oesophageal cancer cell lines. Hyperphosphatemia has been associated with an increased risk of mortality in patients with end-stage renal disease. The aims of this study were to evaluate early auditory perception and speech production skills, and to compare the outcomes between two groups of children wearing the Nucleus cochlear implant (CI) and Clarion CI. Novel linear O-linked saccharides with multiple beta-HexNAc extensions of reducing end Gal were identified. The activity of bCYP51-d1 is similar to that of recombinant human CYP51 with a non-truncated membrane-spanning region. The purpose of this paper was to develop a statistical methodology to optimize tablet manufacturing considering drug chemical and physical properties applying a crossed experimental design. Indeed, more recent experiments have characterised relevant core alpha1-3-fucosylated N-glycan structures that act as epitopes in various model and parasitic organisms. Herein, we report a rare generic zantac recall list case in which bisphosphonate zoledronic acid (ZA) effectively treated not only multiple bone metastases but also lung, pleural and liver metastases from renal cell carcinoma (RCC).

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Reducing electrocardiographic artifacts from electromyogram signals with independent component analysis. Results showed that ISS, BES, and Delta-v were not related to posttraumatic stress symptoms (PTSS) or psychiatric symptoms at 5 and 14 months after the MVA. Reprint of: Assay Validation of the Cardiac Isoform of Troponin I in Double Crested Cormorant (Phalacrocorax auritus) Plasma for Diagnosis of Cardiac Damage. In early egg chambers, pak mutant follicle cells have reduced levels of glucotrol drug classification myosin phosphorylation and we conclude that Pak both promotes and restricts myosin light chain phosphorylation in a temporally distinct manner during oogenesis. We find that the dominant photodissociation mechanism of sulfuric acid below 70 km is absorption in the visible region by OH stretching overtone transitions, whereas above 70 km, absorption of Lyman-alpha radiation by high energy Rydberg excited states is the favored mechanism. Multiple conformational states of proteins: a molecular dynamics analysis of myoglobin. Retention and metabolism of testosterone in the epididymis of viviparous lizards.

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This paper reviews how sex and reproductive hormones interact with circadian and homeostatic sleep regulatory mechanisms in humans and animal models. The activity of cyclophosphamide was increased by a combination with PTZ. In this study, doxorubicin (DOX) was used as the model drug, and a derivative of PHSCN, N-acetyl-proline-histidine-serine-cysteine-asparagine-lysine (amide)-COOH (PHSCNK), was firstly coupled to the surface of PEGylated DOX liposomes (PL-DOX) by a novel approach to obtain the PHSCNK-modified and DOX-loaded PEGylated liposomes (PHSCNK-PL-DOX). These tests must be correlated to target animal protection tests allowing the estimation of the vaccine potency with the same accuracy. Protective effect of the green tea component, L-theanine on environmental toxins-induced neuronal cell death.

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