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November 7, 2025
Brand Name :
Zomax
Synonyms :
Zomepiracum, zomepirac
Class :
Analgesic, Nonnarcotic Analgesic, Nonsteroidal anti-inflammatory agent, Acetic acid derivatives, Prostaglandin synthetase inhibitor
Dosage Forms & StrengthsÂ
TabletÂ
100 mgÂ
It is used to relieve pain and inflammation with a usual recommended dose of 100-200 mg via oral administration can be taken in divided doses
Dose Adjustments
Limited data is available
Safety and efficacy are not seen in pediatricsÂ
Refer to the adult dosingÂ
zomepirac may reduce the elimination rate of abacavir, resulting in a greater serum level
when zomepirac is coupled with acenocoumarol, the risk or severity of bleeding and hemorrhage can be enhanced
when zolmitriptan is taken with zomepirac, the risk or severity of hypertension can be enhanced
when antipyrine is coupled with zomepirac, the risk or severity of undesirable effects can be enhanced
zomepirac may reduce the elimination rate of benzatropine, resulting in a greater serum level
Actions and Spectrum:Â
Actions:Â
The ability of zomepirac, like other nonsteroidal anti-inflammatory medicines (NSAIDs), to block cyclooxygenase (COX) enzymes, notably COX-1 and COX-2, was fundamental to its effect.Â
Spectrum:Â
Zomepirac’s mechanism of action is similar to that of other nonsteroidal anti-inflammatory medicines (NSAIDs) in that it primarily works by inhibiting cyclooxygenase (COX) enzymes and reducing prostaglandin synthesis. Zomepirac has the following actions: anti-inflammatory, analgesic (pain reliever), and antipyretic (fever reducer).Â
Frequency definedÂ
DizzinessÂ
NauseaÂ
Duodenal ulcersÂ
Bloody or tarry stoolsÂ
HeadacheÂ
Stomach painÂ
Heart burnÂ
IndigestionÂ
Liver function abnormalitiesÂ
Skin rashÂ
Hypersensitivity reactionsÂ
ThrombocytopeniaÂ
AnemiaÂ
Kidney damage with over useÂ
Black Box Warning:Â
N/AÂ
Contraindication/Caution:Â
ContraindicationsÂ
CautionsÂ
Pregnancy consideration:Â Â
No data is available regarding the administration of the drug during pregnancy.Â
Breastfeeding warnings:Â Â
No data is available regarding the excretion of drug in breast milk.Â
Pregnancy category:Â
Category A: well-controlled and satisfactory studies show no risk to the fetus in the first or later trimester.Â
Category B: there was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women.Â
Category C: there was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.   Â
Category D: adequate data with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.   Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence these categories of drugs need to be avoided by pregnant women.   Â
Category N: No data is available for the drug under this category.Â
Pharmacology:Â
The pharmacology of zomepirac, a nonsteroidal anti-inflammatory medication (NSAID), was principally connected to its capacity to inhibit cyclooxygenase (COX) enzymes, specifically COX-1 and COX-2.Â
Pharmacodynamics:Â
When it was accessible and prescribed, zomepirac had pharmacodynamic qualities similar to other nonsteroidal anti-inflammatory medications (NSAIDs). Its main pharmacodynamic function was to reduce the activity of cyclooxygenase (COX) enzymes, notably COX-1 and COX-2.Â
Pharmacokinetics:Â
AbsorptionÂ
Zomepirac would have been absorbed from the gastrointestinal system into the bloodstream after oral dosing. The pace and amount of absorption vary between individuals and may be altered by factors such as dietary availability.Â
DistributionÂ
Zomepirac, once in the bloodstream, would have been transported to various tissues throughout the body. NSAIDs, such as zomepirac, have a relatively large volume of distribution, implying that they can permeate tissues, particularly inflamed tissues. MetabolismÂ
Zomepirac would have gone through metabolic processes in the liver, although the specifics of its metabolism are unknown. Metabolites can be formed as a result of metabolism.
Elimination and ExcretionÂ
The elimination half-life of zomepirac varies between people and may be affected by factors such as age, renal function, and liver function. In general, the elimination half-life of NSAIDs is several hours. The kidneys are the primary route of elimination for zomepirac and its metabolites. Factors such as renal function influence the rate of elimination. Some metabolites may be eliminated through the urine.Â
Administration:Â
Typically, zomepirac tablets or capsules were taken with a full glass of water. To lessen the risk of gastrointestinal adverse effects, it is usually best to take the drug with or after a meal. This is also known as “administer with food.” Unless otherwise directed by your healthcare professional, zomepirac tablets or capsules should be swallowed whole, not crushed, chewed, or broken.
Patient information leafletÂ
Generic Name: zomepiracÂ
Pronounced: Zoh-MEP-uh-rackÂ
Why do we use zomepirac?Â
Zomepirac was a nonsteroidal anti-inflammatory medication (NSAID) used to treat pain and inflammation in a variety of medical disorders. The primary indications for zomepirac use were Gout Management, Pain Relief, Anti-Inflammatory Action, and Fever Reduction.Â