Мефенаминка
Мефенаминка Uses, Dosage, Side Effects, Food Interaction and all others data.
Мефенаминка, an anthranilic acid derivative, is a prototypical NSAID. It reversibly inhibits the cyclooxygenase-1 and cyclooxygenase-2 (COX-1 and COX-2) enzymes, thus resulting in reduced synthesis of prostaglandin precursors. It has analgesic and antipyretic properties with minor anti-inflammatory activity.
Мефенаминка, an anthranilic acid derivative, is a member of the fenamate group of nonsteroidal anti-inflammatory drugs (NSAIDs). It exhibits anti-inflammatory, analgesic, and antipyretic activities. Similar to other NSAIDs, mefenamic acid inhibits prostaglandin synthetase.
Trade Name | Мефенаминка |
Generic | Mefenamic acid |
Mefenamic acid Other Names | Acide méfénamique, ácido mefenámico, Acidum mefenamicum, Mefenamic acid, Mefenaminsäure |
Type | |
Formula | C15H15NO2 |
Weight | Average: 241.2851 Monoisotopic: 241.110278729 |
Protein binding | 90% |
Groups | Approved |
Therapeutic Class | Drugs for Osteoarthritis, Drugs used for Rheumatoid Arthritis, Non-steroidal Anti-inflammatory Drugs (NSAIDs) |
Manufacturer | |
Available Country | Ukraine |
Last Updated: | September 19, 2023 at 7:00 am |
![Мефенаминка Мефенаминка](https://www.medicinesfaq.com/media/png/ru-mefenamynka.png)
Uses
Мефенаминка is used in mild to moderate pain including headache, dental pain, postoperative and postpartum pain, dysmenorrhoea, menorrhagia, in musculoskeletal and joint disorders such as osteoarthritis and rheumatoid arthritis; and in children with fever and juvenile idiopathic arthritis.
Мефенаминка is also used to associated treatment for these conditions: Mild pain, Primary Dysmenorrhoea, Gastrointestinal cramps, Moderate Pain
How Мефенаминка works
Мефенаминка binds the prostaglandin synthetase receptors COX-1 and COX-2, inhibiting the action of prostaglandin synthetase. As these receptors have a role as a major mediator of inflammation and/or a role for prostanoid signaling in activity-dependent plasticity, the symptoms of pain are temporarily reduced.
Dosage
Мефенаминка dosage
As with other NSAIDs, the lowest dose should be sought for each patient. Therefore, after observing the response to initial therapy with Мефенаминка, the dose and frequency should be adjusted to suit an individual patient's needs.Administration is by the oral route, preferably with food.
- Adult: A 500 mg dose should be given to adults up to three times (1.5 g total) per day.
- Infants over 6 months: 25 mg/kg of body weight daily in divided doses for not longer than 7 days.
Side Effects
In patients taking Мефенаминка or other NSAIDs, the most frequently reported adverse experiences include : abdominal pain, constipation, diarrhoea, dyspepsia, flatulence, gross bleeding/perforation, heartburn, nausea, GI ulcers, vomiting, abnormal renal function, anaemia, dizziness, oedema, elevated liver enzymes, headache, increased bleeding time, pruritus, rash and tinnitus.
Toxicity
Oral, rat LD50: 740 mg/kg. Symptoms of overdose may include severe stomach pain, coffee ground-like vomit, dark stool, ringing in the ears, change in amount of urine, unusually fast or slow heartbeat, muscle weakness, slow or shallow breathing, confusion, severe headache or loss of consciousness.
Precaution
NSAIDs should be prescribed with extreme caution in those with a prior history of ulcer disease or gastrointestinal bleeding. To minimise the potential risk for an adverse GI event, the lowest effective dose should be used for the shortest possible duration. In cases with pre-existing advanced kidney disease, treatment with Мефенаминка is not recommended.
Interaction
Concomitant use with CYP2C9 isoenzyme inhibitors may alter safety and efficacy of mefenamic acid. May enhance methotrexate toxicity. Reduced BP response to ACE inhibitors or angiotensin II receptor antagonists. Increased risk of serious GI events with aspirin. May reduce the natriuretic effects of furosemide or thiazide diuretics. Reduced renal lithium clearance and elevated plasma lithium levels. May enhance anticoagulant effect of warfarin.
Food Interaction
- Avoid alcohol.
- Take with food.
Volume of Distribution
- 1.06 L/kg [Normal Healthy Adults (18-45 yr)]
Elimination Route
Мефенаминка is rapidly absorbed after oral administration.
Half Life
2 hours
Clearance
- Oral cl=21.23 L/hr [Healthy adults (18-45 yrs)]
Elimination Route
The fecal route of elimination accounts for up to 20% of the dose, mainly in the form of unconjugated 3-carboxymefenamic acid.3 The elimination half-life of mefenamic acid is approximately two hours. Мефенаминка, its metabolites and conjugates are primarily excreted by the kidneys. Both renal and hepatic excretion are significant pathways of elimination.
Pregnancy & Breastfeeding use
Pregnancy: In late pregnancy, as with other NSAIDs, Мефенаминка should be avoided because it may cause premature closure of the ductus arteriosus. In general there are no adequate and well controlled studies in pregnant women. Мефенаминка should be used during pregnancy only if the potential benefit justifies the potential risk to the foetus. Rated as Pregnancy Category C.
Lactation: Trace amounts of Мефенаминка may be present in breast milk. Taking into account the importance of the drug to the mother , decision should be made whether to discontinue nursing or to discontinue the drug.
Contraindication
Мефенаминка is contraindicated in patients with known hypersensitivity to Me Мефенаминка acid. Мефенаминка should not be given to patients who have experienced asthma, urticaria, or allergic type reactions after taking aspirin or other NSAIDs. Rarely fatal, anaphylactic like reactions to NSAIDs have been reported in such patients. Мефенаминка is contraindicated in patients with active ulceration or chronic inflammation of upper gastrointestinal tract and should not be used in patients with preexisting renal disease.
Acute Overdose
Symptoms: Headache, nausea, vomiting, epigastric pain, GI bleeding. Rarely, diarrhoea, disorientation, excitation, coma, drowsiness, tinnitus, fainting, and occasionally convulsions.
Management: Symptomatic and supportive treatment. In acute overdosage, empty the stomach immediately by inducing emesis or by gastric lavage followed by admin of activated charcoal.
Storage Condition
Store between 20-25° C.
Innovators Monograph
You find simplified version here Мефенаминка
Мефенаминка contains Mefenamic acid see full prescribing information from innovator Мефенаминка Monograph, Мефенаминка MSDS, Мефенаминка FDA label
FAQ
What is Мефенаминка used for?
Мефенаминка is used short-term to treat mild to moderate pain in adults and children who are at least 14 years old.
How safe is Мефенаминка?
Мефенаминка may increase your risk of heart problems, including heart attack, stroke, heart failure, or blood clot. These conditions can be fatal. Your risk may increase if you already have heart disease or have taken the medication for a long period of time or at high doses.
How does Мефенаминка work?
Мефенаминка works by stopping the body's production of a substance that causes pain, fever, and inflammation.
What are the common side effects of Мефенаминка?
Common side effects of Мефенаминка are include:
- diarrhea.
- constipation.
- gas or bloating.
- headache.
- dizziness.
- nervousness.
- ringing in the ears
Is Мефенаминка safe during pregnancy?
Use of Мефенаминка during pregnancy is not advised unless prescribed by a doctor, especially if you are 30 or more weeks pregnant.
Is Мефенаминка safe during breastfeeding?
Мефенаминка passes into breast milk and is not recommended for use while breastfeeding.
Can I drink alcohol with Мефенаминка?
Do not drink alcohol while taking Мефенаминка. Alcohol can increase your risk of stomach bleeding caused by Мефенаминка. Call your doctor at once if you have symptoms of bleeding in your stomach or intestines.
Can I drive after taking Мефенаминка?
Мефенаминка Tablets may cause drowsiness, fatigue, dizziness or may affect your vision. If you experience any of these symptoms, you should not drive or operate machinery, or perform any tasks which may require you to be alert.
When should be taken of Мефенаминка?
Мефенаминка is usually taken with food every 6 hours as needed for up to 1 week.
Is it safe to take Мефенаминка?
Мефенаминка should not be used for longer than 7 days.
How many times can I take Мефенаминка?
Мефенаминка take 250 mg every six hours as needed. You shouldn't take Мефенаминка for longer than three days.
How long does Мефенаминка take to work?
If you wait until the symptoms have worsened,Мефенаминка may not work as well. If you are using Мефенаминка for painful periods, take your first dose as soon as your period starts or pain begins. Usually, you will only need to take it for the first 2 to 3 days of your period.
How long does it take for Мефенаминка to kick in?
Мефенаминка takes between 2 - 4 hours to kick in and start easing your period pain. Each 500mg dose of Мефенаминка kills pain for up to 8 hours, so you may need to take it two or three times a day for all-day relief.
Can I take Мефенаминка for a long time?
Мефенаминка should not be used for longer than 7 days. Follow your doctor's dosing instructions very carefully. If you use Мефенаминка long-term, you may need frequent medical tests.Мефенаминка can cause unusual results with certain medical tests.
Who should not take Мефенаминка?
Мефенаминка can increase your risk of fatal heart attack or stroke. Do not use Мефенаминка just before or after heart bypass surgery .Мефенаминка may also cause stomach or intestinal bleeding, which can be fatal.
What happens if I miss a dose on Мефенаминка?
Take Мефенаминка 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 take too much Мефенаминка?
If you take too much If you take too much Мефенаминка, you may experience: drowsiness, nausea,vomiting.
When can I stop taking Мефенаминка?
If you experience any of the following symptoms, stop taking Мефенаминка and call your doctor: stomach pain, heartburn, vomit that is bloody or looks like coffee grounds, blood in the stool, or black and tarry stools.
Can Мефенаминка affects my heart ?
Мефенаминка can increase your risk of fatal heart attack or stroke, especially if you use it long term or take high doses, or if you have heart disease.