Desloratadina Interpharma

Desloratadina Interpharma Uses, Dosage, Side Effects, Food Interaction and all others data.

Desloratadina Interpharma is a long-acting, tricyclic, non-sedating, selective peripheral histamine H1-receptor antagonist which inhibits the release of pro-inflammatory mediators from human mast cells and basophils.

Desloratadina Interpharma is a long-acting second-generation H1-receptor antagonist which has a selective and peripheral H1-antagonist action. Histamine is a chemical that causes many of the signs that are part of allergic reactions, such as the swelling of tissues. Histamine is released from histamine-storing cells (mast cells) and attaches to other cells that have receptors for histamine. The attachment of the histamine to the receptors causes the cell to be "activated," releasing other chemicals which produce the effects that we associate with allergies. Desloratadina Interpharma blocks one type of receptor for histamine (the H1 receptor) and thus prevents activation of cells by histamine. Unlike most other antihistamines, Desloratadina Interpharma does not enter the brain from the blood and, therefore, does not cause drowsiness.

Trade Name Desloratadina Interpharma
Availability Prescription only
Generic Desloratadine
Desloratadine Other Names Descarboethoxyloratadine, Desloratadina, Desloratadine
Related Drugs prednisone, cetirizine, loratadine, fluticasone nasal, promethazine, diphenhydramine, Zyrtec, Xolair
Type
Formula C19H19ClN2
Weight Average: 310.821
Monoisotopic: 310.123676325
Protein binding

Desloratadine is bound approximately 82 to 87% to plasma proteins, while its active metabolite, 3-hydroxydesloratadine, is bound approximately 85 to 89%.

Groups Approved, Investigational
Therapeutic Class Non-sedating antihistamines
Manufacturer
Available Country Chile
Last Updated: September 19, 2023 at 7:00 am
Desloratadina Interpharma
Desloratadina Interpharma

Uses

Allergic Rhinitis: Desloratadina Interpharma is used for the relief of the nasal and non-nasal symptoms of allergic rhinitis (Both seasonal and perennial) in patients 2 years of age and older.

Chronic Idiopathic Urticaria: Desloratadina Interpharma is also used for the symptomatic relief of pruritus, reduction in the number of hives, and size of hives, in patients with chronic idiopathic urticaria 2 years of age and older.

Desloratadina Interpharma is also used to associated treatment for these conditions: Allergic Rhinitis (AR), Asthma, Chronic Idiopathic Urticaria, Common Cold, Nasal Congestion, Perennial Allergic Rhinitis (PAR), Seasonal Allergic Rhinitis, Nasal symptoms, Non-nasal symptoms, Antihistamine

How Desloratadina Interpharma works

Like other H1-blockers, Desloratadina Interpharma competes with free histamine for binding at H1-receptors in the GI tract, uterus, large blood vessels, and bronchial smooth muscle. This blocks the action of endogenous histamine, which subsequently leads to temporary relief of the negative symptoms (eg. nasal congestion, watery eyes) brought on by histamine.

Dosage

Desloratadina Interpharma dosage

Pediatric drops :

  • Child 6 -11 months of age: 2 ml drops once daily
  • Child 1 -2 years of age: 2.5 ml drops once daily

Syrup:

  • Child 6-11 months of age: 2 ml once daily
  • Child 1-5 years of age: 2.5 ml once daily
  • Child 6-11 years of age: 5 ml once daily
  • Adults & > 12 years of age: 10 ml once daily

Tablet:

  • Adults and children 12 years of age and over: 5 mg daily

Side Effects

Desloratadina Interpharma is generally well tolerated. However, dry mouth, fatigue, somnolence and myalgia are commonly reported side-effects. Less common side-effects may include dizziness, headache and nausea. Rarely rash, pruritus and urticaria may occur.

Toxicity

Information regarding desloratadine overdose is limited, although somnolence has been reported. In case of overdose, symptomatic and supportive treatment, including removing the unabsorbed drug, is recommended; note, however, that desloratadine and its active metabolite 3-hydroxydesloratadine cannot be eliminated by hemodialysis.

In animal studies, lethality was observed at or above doses of 250 mg/kg in rats and of 353 mg/kg in mice (oral LD50), doses that represent 120 and 290 times the human exposure based on the recommended daily oral dose. In monkey, no deaths occurred at doses up to 250 mg/kg, representing an exposure roughly 810 times that of the recommended dose in humans.

Precaution

Hepatic and renal impairment. Pregnancy and lactation.

Interaction

Concomitant administration of Erythromycin, Ketoconazole, Azithromycin, Fluoxetine, and Cimetidine with Desloratadina Interpharma increased the plasma concentration of Desloratadina Interpharma. But there were no clinically relevant changes in the safety profile of Desloratadina Interpharma.

Food Interaction

  • Take with or without food. The absorption is unaffected by food.

Desloratadina Interpharma Disease Interaction

Moderate: asthma, renal/hepatic impairment

Elimination Route

Desloratadina Interpharma administered orally for ten days to healthy volunteers as a 5 mg tablet once daily resulted in a mean Tmax of approximately 3 hours, a mean steady-state Cmax of 4 ng/ml, and a mean steady-state AUC of 56.9 ng*hr/ml. A similar profile was observed using 10 ml of an oral solution containing 5 mg of desloratadine. Food was found not to affect desloratadine absorption.

Half Life

Desloratadina Interpharma has a mean plasma elimination half-life of approximately 27 hours.

Elimination Route

Approximately 87% of a C-desloratadine dose was equally recovered in urine and feces as metabolic products.

Pregnancy & Breastfeeding use

Pregnancy: There are no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, Desloratadina Interpharma should be used in pregnancy only if clearly needed.

Lactation: Desloratadina Interpharma passes into breast milk. Therefore, a decision should be made whether to discontinue nursing or to discontinue Desloratadina Interpharma, taking into account the importance of the drug to the mother.

Contraindication

Desloratadina Interpharma is contraindicated in patient having hypersensitivity to this medication or to any of its ingredients or Loratadine.

Special Warning

Paediatric Use: The safety and effectiveness of Desloratadina Interpharma in pediatric patients under 2 years of age have not been established.

Geriatric Use: In general, dose selection for an elderly patient should be cautious, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.

In adult patients with liver or renal impairment: A starting dose of one 5 mg tablet every other day is recommended based on pharmacokinetic data.

Acute Overdose

No clinically relevant adverse events have been reported in case of overdosage. However, in the event of overdosage, symptomatic and supportive treatment is recommended.

Storage Condition

Store in a cool and dry place, protected from light.

Innovators Monograph

You find simplified version here Desloratadina Interpharma

Desloratadina Interpharma contains Desloratadine see full prescribing information from innovator Desloratadina Interpharma Monograph, Desloratadina Interpharma MSDS, Desloratadina Interpharma FDA label

FAQ

What is Desloratadina Interpharma used for?

Desloratadina Interpharma is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose, itching eyes/nose, sneezing, hives, and itching. Desloratadina Interpharma is used to treat allergies. It is an active metabolite of loratadine. It is used to relieve the symptoms of hay fever and hives of the skin.

How safe is Desloratadina Interpharma?

Desloratadina Interpharma is a safe and effective treatment for allergic diseases.

How does Desloratadina Interpharma work?

Desloratadina Interpharma works by blocking histamine, a substance in the body that causes allergic symptoms.

What are the common side effects of Desloratadina Interpharma?

Common side effects of Desloratadina Interpharma are include:

  • headache.
  • nausea.
  • diarrhea.
  • dizziness.
  • sore throat.
  • dry mouth.
  • muscle pain.
  • extreme tiredness

Is Desloratadina Interpharma safe during pregnancy?

As such these findings provide reassurance by indicating that the fetal safety of Desloratadina Interpharma is similar to the currently recommended antihistamines during pregnancy and thus Desloratadina Interpharma can be considered to be another option for use during pregnancy.

Is Desloratadina Interpharma safe during breastfeeding?

Considering the minimal exposure of a nursing infant to the drugs through breast milk, maternal use of Desloratadina Interpharma dose is unlikely to result in adverse effects in nursing infants and is considered to be compatible with breastfeeding.

Can I drink alcohol with Desloratadina Interpharma?

Desloratadina Interpharma alone or in combination with alcohol was safe and well tolerated.

Can I drive after taking Desloratadina Interpharma?

Do not drive and do not use tools or machines.

When should be taken of Desloratadina Interpharma?

You can take Desloratadina Interpharma before or after meals.

Can I take Desloratadina Interpharma every day?

The recommended dose of Desloratadina Interpharma tablets is one 5 mg tablet once daily.

How long does Desloratadina Interpharma take to work?

Desloratadina Interpharma is also use to relieve the symptoms of allergic skin conditions  such as skin itch and hives. Desloratadina Interpharma usually starts to work within 75 minutes and lasts for 24 hours.

What is the half-life of Desloratadina Interpharma ?

The 27-hour half-life of Desloratadina Interpharma permits once daily administration.

How long can I take Desloratadina Interpharma for?

You can limit treatment to 14 days.

Can I take Desloratadina Interpharma for a long time?

Desloratadina Interpharma is unlikely to do you any harm if you take it for a long time. However, it's best to take it only for as long as you need to. It's best not to drink alcohol while you're taking Desloratadina Interpharma, as it can make you feel sleepy.

Who should not take Desloratadina Interpharma?

Follow all directions on your medicine label and package. Tell each of your healthcare providers about all your medical conditions, allergies, and all medicines you use.

What happens if I miss a dose?

Take the medicine as soon as you can, but skip the missed dose if it is almost time for your next dose. Do not take two doses at one time.

What happen if I overdose of Desloratadina Interpharma?

tiredness. sleepiness. menstrual pain. Increased sleepiness or tiredness can happen if you take more Desloratadina Interpharma than your doctor prescribed to you.

Can Desloratadina Interpharma cause infertility?

Desloratadina Interpharma is not expected to cause other pregnancy problems.

Does Desloratadina Interpharma increase blood pressure?

The decongestant in Desloratadina Interpharma  and pseudoephedrine may cause blood pressure to increase and may also speed up the heart rate.

Can Desloratadina Interpharma affects my kidney?

Older patients are more likely to have kidney or liver problems which may make them more sensitive to the effects of Desloratadina Interpharma. Your doctor may give you a different Desloratadina Interpharma dose if you have kidney or liver problems.

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*** Taking medicines without doctor's advice can cause long-term problems.
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