Loratadine Teva
Loratadine Teva Uses, Dosage, Side Effects, Food Interaction and all others data.
Loratadine Teva is a non-sedating antihistamine. It works by selectively binding to peripheral histamine H1-receptors on effector cells.
Like other 2nd generation antihistamines, loratadine is selective for peripheral H1 receptors. Loratadine Teva does not penetrate effectively into the central nervous system and has poor affinity for CNS H1-receptors. These qualities result in a lack of CNS depressant effects such as drowsiness, sedation, and impaired psychomotor function.
Trade Name | Loratadine Teva |
Availability | Rx and/or OTC |
Generic | Loratadine |
Loratadine Other Names | Loratadina, Loratadine, Loratadinum |
Related Drugs | prednisone, hydroxyzine, cetirizine, fluticasone nasal, montelukast, promethazine, diphenhydramine, triamcinolone, Benadryl, Zyrtec |
Type | |
Formula | C22H23ClN2O2 |
Weight | Average: 382.883 Monoisotopic: 382.144805697 |
Protein binding | 97 - 99% of the loratadine is bound to plasma proteins. |
Groups | Approved, Investigational |
Therapeutic Class | Non-sedating antihistamines |
Manufacturer | |
Available Country | Belgium, France, Hong Kong, Israel |
Last Updated: | September 19, 2023 at 7:00 am |
![Loratadine Teva Loratadine Teva](https://www.medicinesfaq.com/media/png/loratadine-teva.png)
Uses
Loratadine Teva provides faster relief from the symptoms of hay fever, allergic rhinitis such as sneezing, nasal discharge, itching, ocular itching and burning, nasal and ocular sign and symptoms are relieved rapidly after oral administration.
Loratadine Teva is also effective in idiopathic chronic urticaria. In children over 2 years, Loratadine Teva is used for the symptomatic relief of seasonal allergic rhinitis and allergic skin conditions such as urticaria nettle rash.
Loratadine Teva is also used to associated treatment for these conditions: Allergic Dermatologic Disorders, Allergic Rhinitis (AR), Allergies, Chronic Urticaria, Common Cold, Eye pruritus, Fever, Nasal Congestion, Nasal Itching, Pain, Perennial Allergic Rhinitis (PAR), Perennial Rhinitis, Pollen Allergy, Pruritus, Rhinorrhoea, Seasonal Allergic Rhinitis, Sneezing, Sensation of burning in the eyes, Watery eyes, Watery itchy eyes
How Loratadine Teva works
Histamine release is a key mediator in allergic rhinitis and urticaria. As a result, loratadine exerts it's effect by targeting H1 histamine receptors.
Loratadine Teva binds to H1 histamine receptors found on the surface of epithelial cells, endothelial cells, eosinophils, neutrophils, airway cells, and vascular smooth muscle cells among others. H1 histamine receptors fall under the wider umbrella of G-protein coupled receptors, and exist in a state of equilibrium between the active and inactive forms. Histamine binding to the H1-receptor facilitates cross linking between transmembrane domains III and V, stabilizing the active form of the receptor. On the other hand, antihistamines bind to a different site on the H1 receptor favouring the inactive form.
Hence, loratadine can more accurately be classified as an "inverse agonist" as opposed to a "histamine antagonist", and can prevent or reduce the severity of histamine mediated symptoms.
Dosage
Loratadine Teva dosage
Adult & children over 12 years of age: One Loratadine Teva 10 mg tablet once daily (usually in the morning).
Children:
- 2-12 years (body weight more than 30 Kg): 10 mg Loratadine Teva once daily.
- 2-12 years (body weight less than 30 Kg): 5 mg Loratadine Teva once daily.
- Below 2 years of age: Safety and efficacy of Loratadine Teva have not been established.
Liver & renal impairment: Patients with liver impairment and renal insufficiency (GFR <30 ml/min) should be given a lower initial dose (10 mg every other day).
Side Effects
Fatigue, nausea and headache were reported rarely. Scientific studies showed that Loratadine Teva does not cause drowsiness. It does not affect performance and ability to drive or tasks requiring concentration.
Toxicity
Second generation antihistamines such as loratadine have very few adverse effects; however, insomnia, headache, fatigue, drowsiness and rash have been reported. Symptoms of loratadine overdose include gastrointestinal side effects, agitation, drowsiness, tachycardia, and headache. It is advised to obtain an ECG in the event of loratadine overdose.
Precaution
Patients with liver impairment and renal insufficiency (GFR <30 ml/min) should be given a lower initial dose (10 mg every other day).
Interaction
When administered concurrently with alcohol, Loratadine Teva has no potentiating effect as measured by psychomotor performance studies. Interactions with other drugs have not been reported.
Food Interaction
No interactions found.[Minor] Theoretically, grapefruit juice may increase the plasma concentrations of loratadine as it does other drugs that are substrates of the CYP450 3A4 enzymatic pathway.
The proposed mechanism is inhibition of CYP450 3A4-mediated first-pass metabolism in the gut wall by certain compounds present in grapefruits.
The clinical significance of this potential interaction is unknown.
Reported interactions with potent CYP450 3A4 inhibitors like clarithromycin, erythromycin and ketoconazole have produced substantial increases in the area under the plasma concentration-time curve (AUC) of loratadine and its active metabolite, descarboethoxyloratadine, without associated changes in the overall safety profile of the drug.
Loratadine Teva Drug Interaction
Unknown: fluticasone / salmeterol, aspirin, aspirin, diphenhydramine, ubiquinone, duloxetine, omega-3 polyunsaturated fatty acids, fluticasone nasal, pregabalin, metoprolol, metoprolol, polyethylene glycol 3350, albuterol, montelukast, budesonide / formoterol, levothyroxine, acetaminophen, cyanocobalamin, ascorbic acid, cholecalciferol
Loratadine Teva Disease Interaction
Volume of Distribution
The volume of distribution of loratadine is 120 L/Kg.
Elimination Route
Loratadine Teva is rapidly absorbed and achieves peak plasma concentration in 1-2 hours, while it's main metabolite achieves peak plasma concentration in 3-4 hours.
In the rapid dissolve formulation, the pharmacokinetic parameters of loratadine are as follows: Cmax = 2.56 ng/ml, Tmax = 1.14 hrs, AUC = 6.14 ng x hr/ml.
In the rapid dissolve formulation, the pharmacokinetic parameters of descarboethoxyloratadine are as follows: Cmax = 3.72 ng/ml, Tmax = 1.97 hr, AUC = 49.1 ng x hr/ml.
In the conventional formulation, the pharmacokinetic parameters of loratadine are as follows: Cmax = 2.11 ng/ml, Tmax = 1.00 hr, AUC = 4.64 ng x hr/ml
In the conventional formulation, the pharmacokinetic parameters of descarboethoxyloratadine are as follows: Cmax = 3.66 ng/ml, Tmax = 1.97 hr, AUC = 48.4 ng x hr/ml
Half Life
The elimination half life is approximately 10 hours for loratadine and 20 hours for descarboethoxyloratadine.
Clearance
The clearance of loratadine after single oral doses of 20 mg and 40 mg are 12 L/h/kg and 9 L/h/kg respectively. P-glycoprotein is involved in the clearance of many 2nd generation antihistamines, including loratadine, from the central nervous system. 1st generation antihistamines are not cleared by P-glycoprotein, which may help explain why they have a different central nervous system adverse effect profile compared to their 2nd generation counterparts. It appears that an antihistamine with higher affinity for p-glycoprotein will have a lower incidence of CNS adverse effects.
Elimination Route
Over a 10 day period, 40% of loratadine is excreted in the urine, and 42% is eliminated in the faeces.
Pregnancy & Breastfeeding use
Use in pregnancy: There is no experience of the use of Loratadine Teva in human pregnancy, hence it should not be used during pregnancy.
Use in lactation: Loratadine Teva is excreted in breast milk, so it should not be administered to lactating mother.
Contraindication
Loratadine Teva is contraindicated in patients who have shown hypersensitivity or idiosyncracy to their components.
Acute Overdose
Symptoms: Somnolence, tachycardia headache, drowsiness, extrapyramidal manifestations and palpitations.
Management: Symptomatic and supportive treatment. Immediately empty stomach by inducing emesis with ipecac syrup. Admin of activated charcoal after emesis may be useful. If induction of vomiting is unsuccessful or contraindicated (e.g. patient is comatose, having seizures or lacks gag reflex), gastric lavage with NaCl 0.9% soln may be performed to prevent aspiration of gastric contents. Saline cathartics may be useful to rapidly dilute bowel contents.
Storage Condition
Store between 20-25° C.
Innovators Monograph
You find simplified version here Loratadine Teva
Loratadine Teva contains Loratadine see full prescribing information from innovator Loratadine Teva Monograph, Loratadine Teva MSDS, Loratadine Teva FDA label
FAQ
What is Loratadine Teva used for?
Loratadine Teva is used to treat sneezing, runny nose, watery eyes, hives, skin rash, hay fever, itching, and other cold or allergy symptoms. It's also used to treat hay fever.
How safe is Loratadine Teva?
Generally, it's considered safe to use Loratadine Teva for a long time, but you should only take it if you need it.Depending on your condition, you may only need to use Loratadine Teva for a short period of time, or you might need to take it longer to treat stubborn allergies.
How does Loratadine Teva work?
Loratadine Teva works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
What are the common side effects of Loratadine Teva?
Common side effects of Loratadine Teva are include:
- headache
- dry mouth
- nosebleed
- sore throat
- mouth sores
- difficulty falling asleep or staying asleep
- nervousness
- weakness
- stomach pain
- diarrhea
- red or itchy eyes
Is Loratadine Teva safe during pregnancy?
Loratadine Teva can be taken in pregnancy. There is no good evidence that it can harm your baby.
Is Loratadine Teva safe during breastfeeding?
Considering the minimal exposure of a nursing infant to the drugs through breast milk, maternal use of Loratadine Teva in a standard therapeutic dose is unlikely to result in adverse effects in nursing infants and is considered to be compatible with breastfeeding.
Can I drink alcohol with Loratadine Teva?
If you take an allergy medication like Loratadine Teva, you may be at risk of drowsiness and confusion if you drink alcohol.
Can I drive after taking Loratadine Teva?
Loratadine Teva is classed as a non-drowsy antihistamine but it's still possible to feel sleepy after taking it. If this happens to you, do not drive a car or ride a bike until you feel better.
When is the best time to take Loratadine Teva?
Take Loratadine Teva once a day at the same time each day, either in the morning or in the evening. You can take Loratadine Teva with or without food.
Is it safe to take Loratadine Teva every day?
Loratadine Teva is safe to take daily.
Can I take Loratadine Teva on an empty stomach?
You may take Loratadine Teva with food or on an empty stomach.
How long does Loratadine Teva take to work?
Usually, Loratadine Teva tablets start to work within 30 minutes after being taken and tend to be most effective within 1-2 hours after being taken.
How long does Loratadine Teva stay in my system?
The elimination half-life of Loratadine Teva is 8–14 hours and that of its metabolite is 17–24 hours, which accounts for the 24-hour duration of action of the drug. Wheal inhibition is detected at 1.5 hours after administration, reaches a peak at 4–6 hours, and may last 36–48 hours.
Can I take Loratadine Teva for a long time?
Yes, you can take Loratadine Teva daily and long term. Loratadine Teva is an antihistamine used to treat for allergy symptoms. If your symptoms are year round then it is able to be taken long term. If your symptoms are seasonal or you have allergy symptoms occasionally, then it is taken daily when required.
Who should not take Loratadine Teva?
You should not take Loratadine Teva if you have any symptom of bellow:
- liver failure.
- liver problems.
- moderate to severe kidney impairment.
What happens if I miss a dose?
Loratadine Teva is used when needed. Do not use Loratadine Teva more than once in a 24-hour period. Do not use two doses at one time.
What happens if I overdose on Loratadine Teva?
Overdose symptoms may include headache, drowsiness, and fast or pounding heartbeat.Seek emergency medical attention.
How quickly does Loratadine Teva work?
Loratadine Teva reaches peak plasma concentration in 1-2 hours; the metabolite does so in 3-4 hours. Their respective elimination half-lives are about 10 and 20 hours. Onset of action is within 1 hour and duration is at least 24 hour.
Can Loratadine Teva affect fertility?
They found Loratadine Teva could have negative long-term side effects for male fertility.
Is Loratadine Teva safe for heart patients?
Newer Loratadine Teva like Loratadine Teva are all fairly safe for the heart, with fexofenadine seeming to be the absolute safest if you are at risk of arrythmia.
Does Loratadine Teva affect blood pressure?
Loratadine Teva increase your blood pressure and heart rate.
Can Loratadine Teva affects my liver?
Patients with liver disease may be at greater risk for adverse effects from Loratadine Teva due to drug and metabolite accumulation. The manufacturer recommends one-half the regular dosage initially in patients with liver failure or decreased renal function.
Can I just stop taking Loratadine Teva?
Exposure to substances such as pollen, pet fur, house dust or insect bites can cause your body to produce allergic symptoms. Cells in the lining of your nose and eyes release histamine when they come into contact with these substances.