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Allergesic (Desloratadine)

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Allergesic is a non-drowsy, once-daily medication used for allergy relief and chronic hives. Unlike most other allergy medications, it is not available over-the-counter. Allergesic is an antihistamine. It blocks the action of histamine, a chemical that causes sneezing, itching, and other allergy symptoms.

Other names for this medication:
Alerdain, Alerta, Allerdain, Allerde, Allerede, Allergesic, Antialer, Biomon, Dazit, Delorta, Descare, Desent, Deslor, Desloranid, Desloratadine, Desloriv, Desnova, Dilora, Lorday, Loreta, Nelora, Neoloridin, Nucope, Otrivin, Reditabs, Rodera, Tastylora, Veromon

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Also known as: Desloratadine


Generic Allergesic is a perfect remedy, which helps to fight against the symptoms of allergies. Its target is to treat sneezing, itching, watery eyes, and runny nose. Generic Allergesic acts by lowering the natural chemical histamine in the body. It is antihistamine. Allergesic is also known as Desloratadine, Dezlorid, NeoClarityn, Claramax, Aerius. Generic name of Generic Allergesic is Desloratadine. Brand names of Generic Allergesic are Allergesic, Allergesic Reditabs.


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

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 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. The tablet will dissolve in seconds, and you may swallow it with your saliva. You do not need to drink water or other liquid to swallow the tablet.

For patients using the syrup form of this medicine: Use a calibrated measuring dropper or syringe to measure the direct dose for your child based on your doctor's instructions. Do not use a regular teaspoon. If you are unsure about how much of the syrup to give to your child, ask your doctor or pharmacist.

For oral dosage form (oral disintegrating tablets): For symptoms of chronic hives: Adults and children 12 years of age and older—5 milligrams (mg) once a day. Children 6 to 11 years of age—2.5 mg once 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 symptoms of hay fever: Adults and children 12 years of age and older—5 mg once a day. Children 6 to 11 years of age—2.5 mg once 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 (tablets): For symptoms of chronic hives: Adults and children 12 years of age and older—5 mg once a day. Children 4 to 12 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 symptoms of hay fever: Adults and children 12 years of age and older—5 mg once a day. Children 4 to 12 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 (syrup): For symptoms of chronic hives: Adults and children 12 years of age and older—2 teaspoonfuls (5 milligrams [mg] in 10 milliliters [mL]) once a day. Children 6 to 11 years of age—1 teaspoonful (2.5 mg in 5 mL) once a day Children 4 to 5 years of age—½ teaspoonful (1.25 mg in 2.5 mL) once a day Children and infants up to 4 years of age—Use is not recommended . For symptoms of hay fever: Adults and children 12 years of age and older—2 teaspoonfuls (5 milligrams [mg] in 10 milliliters [mL]) once a day. Children 6 to 11 years of age—1 teaspoonful (2.5 mg in 5 mL) once a day Children 4 to 5 years of age—½ teaspoonful (1.25 mg in 2.5 mL) once a day Children and infants up to 4 years of age—Use is not recommended .


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

Overdose may cause anxiety, trouble sleeping, headache, vomiting, thirst, muscle weakness, fast or pounding heartbeats, hallucinations, shallow breathing, or a seizure.


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 Desloratadine/pseudoephedrine dosage information

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The most common side effects associated with Allergesic 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.


The elderly are usually more sensitive to the effects of this medicine, especially if it contains:

Antihistamines—Confusion, difficult or painful urination, dizziness, drowsiness, feeling faint, or dryness of mouth, nose, or throat may be more likely to occur in elderly patients. Also, nightmares or unusual excitement, nervousness, restlessness, or irritability may be more likely to occur in the elderly taking antihistamines. Decongestants (e.g., ephedrine, phenylephrine, pseudoephedrine—Confusion, hallucinations, drowsiness, or convulsions (seizures) may be more likely to occur in the elderly, who are usually more sensitive to the effects of this medicine. Also, increases in blood pressure may be more likely to occur in elderly persons taking decongestants.

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Insulin and tolbutamide in the doses applied moderately lowered blood sugar level, whereas buformin did not, thus tolbutamide-induced potentiation may be due to insulin release. QICAR has the potential to complement existing epidemiologic methods for estimating associations between CVDs and air pollutant exposures by providing clues about the underlying mechanisms that may explain these associations. To evaluate pulse type technology used to remove lens fragments during phacoemulsification. Rituximab, a chimeric anti-CD20 monoclonal antibody, in the treatment of B-cell lymphoma. We tested whether chemoreflex sensitivity could be affected by the practice of yoga, and whether this is specifically because of a slow breathing rate obtained during yoga or as a general consequence of yoga. The methylene blue solution for staining of actinospore processes and estimating of daughter cells of sporoplasm is proposed. Owing to a shorter catheterization time, reduced hospital duration and less complication, PVP could be used as an alternative and a promising minimal invasive surgical procedure for the treatment of BPH. However, it appears to increase the uterine artery blood flow bilaterally, and these alterations in the bilateral uterine artery blood flow may be associated with a physiological adaptation to high altitude. Construction of ligand-responsive microRNAs that operate through inhibition of Drosha processing. Surprisingly, in addition to smooth muscle cells, MPhis in diseased arteries also produce the elastin precursor tropoelastin, as shown by double immunostaining, in situ hybridization, and reverse transcription-polymerase chain reaction for tropoelastin mRNA.

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Cell viability was determined according to mitochondrial enzyme activity (3-(4,5- dimethyl-2-thiazoyl)-2,5-diphenyl-2H-tetrazolium bromide assay). Spinal cord stimulation facilitates functional walking in a chronic, incomplete spinal cord injured. Mean aminoterminal B-type natriuretic peptide concentrations in the CHD group were significantly higher on the second (14191 vs. Patients with end-stage achalasia, characterized by tortuous megaesophagus were selected. The observation of TWA hastening ventricular tachyarrhythmias in an extraordinary variety of clinical and experimental conditions suggest potential universality of TWA in the pathophysiological mechanism of sudden death. With this object in mind, this study was undertaken to assess the effects of disrupting the blood supply of the baboon mandible by means of L- and C-osteotomies. There is a possibility that the reported clinical effects of tolterodine arise through the suppression of fluid consumption. This contact was shown to be inhibited by the introduction of neutralizing antibodies to MIP-1alpha and MIP-1beta. As the prophylactic measures, chemoprophylaxis is recommended where there is no history of TB treatment and healing of tuberculosis has been found on chest X-ray films. Inflammatory biomarkers and spontaneous preterm birth among obese women.

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