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Brand Name :
Maxicam
Synonyms :
isoxicam, Isoxicamo, Isoxicamum
Class :
Anti-inflammatory, Nonsteroidal anti-inflammatory drug (NSAID), Oxicams, Non-selective inhibitor of COX (1 and 2)
Dosage Forms & StrengthsÂ
TabletÂ
100 mgÂ
200 mgÂ
250 mgÂ
300 mg      Â
Isoxicam, a nonsteroidal anti-inflammatory agent, is predominantly utilized for treating conditions like rheumatoid arthritis and degenerative joint disease
The metabolism of [14C]-isoxicam was studied in normal, healthy adult male volunteers after the administration of a single daily oral dose of 300 mg
Dose Adjustments
Limited data is available
Safety and efficacy are not seen in pediatricsÂ
Refer to the adult dosingÂ
isoxicam leads to a reduction in the rate of excretion of nitric oxide, which leads to an increased level of serum
When isoxicam is used together with nifenazone, this leads to enhanced risk or seriousness of adverse events
When isoxicam is used together with diazoxide, this leads to reduction in therapeutic effectiveness of diazoxide
SSRIs increase the antiplatelet effect of NSAIDs
choline magnesium trisalicylate
may enhance the adverse/toxic effect of salicylates
may enhance the risk or severity of hypertension when combined
isoxicam might reduce the excretion rate of abacavir, leading to a potential elevation in serum levels
the risk of bleeding and hemorrhage may increase when isoxicam is combined with abciximab
isoxicam may diminish the acebutol's antihypertensive effects
the risk of adverse effects could be heightened when aceclofenac is combined with isoxicam
combining isoxicam with acemetacin may increase the risk or severity of adverse effects
the risk of bleeding and hemorrhage may increase when isoxicam is combined with acenocoumarol
isoxicam may increase the risk or severity of adverse effects when combined with acetaminophen
the protein binding of acetohexamide may decrease when combined with isoxicam
the risk of adverse effects may increase when acetylsalicylic acid is combined with isoxicam
isoxicam may reduce the excretion rate of aclidinium, potentially leading to a higher serum level
combining isoxicam with zoledronic acid may raise the risk of gastrointestinal bleeding
the risk or severity of hypertension may increase when zolmitriptan is combined with isoxicam
isoxicam may increase the risk or severity of hyperkalemia when combined with zonisamide
combining isoxicam with zuclopenthixol may increase the risk or severity of hypertension
the risk or severity of hyperkalemia may increase when isoxicam is combined with trimebutine
the risk or severity of hyperkalemia may increase when trimethadione is combined with isoxicam
isoxicam may increase the risk or severity of hyperkalemia when combined with trimethoprim
isoxicam might reduce the excretion rate of trimetrexate, potentially leading to a higher serum level
combining trimipramine with isoxicam may increase the risk or severity of gastrointestinal bleeding
the risk or severity of adverse effects may increase when isoxicam is combined with trolamine salicylate
isoxicam may reduce the excretion rate of tropisetron, potentially leading to a higher serum level
isoxicam may enhance the neuroexcitatory activities of trovafloxacin
the therapeutic efficacy of unoprostone may be reduced when used in combination with isoxicam
Actions and Spectrum:Â
Actions:Â
Isoxicam is a non-steroidal anti-inflammatory agent designed for arthritis research, exhibiting oral activity and a prolonged duration of action. It functions as a nonselective inhibitor of both COX-1 and COX-2.Â
Spectrum:Â
A non-steroidal anti-inflammatory drug (NSAID) with anti-inflammatory properties that doesn’t belong to the steroid category. Aside from their anti-inflammatory effects, NSAIDs also exhibit analgesic, antipyretic, and platelet-inhibitory actions. These medications work by suppressing the enzyme cyclooxygenase, which is involved in the synthesis of prostaglandins. This prevents arachidonic acid from being converted into cyclic endoperoxides, which are the building blocks of prostaglandins.Â
Frequency not definedÂ
Vomiting Â
Nausea Â
Headache Â
Ulcers Â
Increased risk of bleeding or bruising, perforation (GI issues)Â Â
Exacerbation of respiratory problems Â
Dizziness Â
Steven’s johnson syndrome Â
Heart attack or stroke Â
Increased BPÂ
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Black Box Warning:Â
The use of NSAIDs, including isoxicam, may elevate the likelihood of severe gastrointestinal complications, such as bleeding, ulceration, and perforation in the stomach or intestines, with the potential for fatal outcomes.Â
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
Isoxicam is a nonselective inhibitor of cyclooxygenase enzymes, particularly COX-1 and COX-2. These enzymes are in charge of converting arachidonic acid into prostaglandins, which are essential for the treatment of fever, discomfort, and inflammation.Â
Pharmacodynamics:Â
The pharmacodynamics of isoxicam involves understanding how the drug interacts with the body’s physiological systems and produces its therapeutic effects. Here are key aspects of the pharmacodynamics of isoxicam:Â
Cyclooxygenase Inhibition: Isoxicam is a nonsteroidal anti-inflammatory drug (NSAID) that inhibits the activity of cyclooxygenase (COX) enzymes. Arachidonic acid is converted by COX enzymes into prostaglandins, which are messengers of fever, pain, and inflammation.Â
COX-1 and COX-2 Inhibition: Isoxicam is a nonselective COX inhibitor, meaning it affects both COX-1 and COX-2 isoforms. COX-1 is constitutively expressed and involved in normal physiological functions, including gastric mucosal protection and platelet aggregation. Induced during inflammation, COX-2 aids in the production of prostaglandins that cause inflammation and pain.Â
Prostaglandin Reduction: By inhibiting COX, isoxicam reduces the synthesis of prostaglandins. Prostaglandins are signaling molecules that mediate inflammation, sensitize pain receptors, and contribute to the fever response. The decrease in prostaglandin levels results in anti-inflammatory, analgesic, and antipyretic effects.Â
Anti-Inflammatory Effects: Isoxicam’s primary pharmacodynamic effect is the attenuation of the inflammatory response. This is particularly relevant in conditions such as rheumatoid arthritis and osteoarthritis, where inflammation plays a key role in disease progression.Â
Analgesic Effects: Isoxicam provides pain relief by reducing the production of prostaglandins involved in pain sensitization and transmission. This contributes to its analgesic properties, making it effective in alleviating pain associated with inflammatory conditions.Â
Antipyretic Effects: Through the inhibition of prostaglandins, isoxicam helps lower elevated body temperature associated with fever.Â
Platelet Function: Isoxicam, as a nonselective COX inhibitor, affects platelet function by reducing the synthesis of thromboxane, a prostaglandin involved in platelet aggregation. This can result in an antiplatelet effect, potentially influencing blood clotting.Â
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Pharmacokinetics:Â
AbsorptionÂ
Bioavailability is 97-+11%Â
The time to achieve peak effect is 10 hoursÂ
DistributionÂ
The volume of distribution is 12.7 L/kgÂ
MetabolismÂ
Undergoes hepatic metabolism.Â
Elimination and ExcretionÂ
The half-life is 10.5-53.9 hours and excretion via urine.Â
Administration:Â
Isoxicam is typically administered orally through tablets or capsules. Here are some general guidelines for its use:Â
Dosage: The recommended dosage of isoxicam may vary depending on the specific formulation, the treated condition, and individual patient factors. Always adhere to the dosage instructions provided by your healthcare provider.Â
Frequency: Isotoxicam is usually taken once daily, although the exact frequency may be influenced by the specific prescription and medical condition.Â
Timing: To minimize the risk of gastrointestinal irritation, it is often advised to take isoxicam with food or after a meal.Â
Swallow Whole: Ingest the tablet or capsule whole with a full glass of water. Avoid crushing, breaking, or chewing the medication unless otherwise instructed by your healthcare provider.Â
Consistency: Maintain a consistent schedule by taking isoxicam at the same time each day to ensure a steady level of the medication in your system.Â
Duration of Use: Use isoxicam for the duration prescribed by your healthcare provider. Even if your symptoms become better, you should still talk to your doctor before stopping the prescription.Â
It’s necessary to communicate with your healthcare provider about other medications, supplements, or medical conditions before starting isoxicam. Your overall health profile will be considered to determine the appropriate dosage, and your healthcare provider will monitor for side effects.Â
As with any medication, strict adherence to your doctor’s instructions is crucial. If you have concerns or experience unusual symptoms, seek medical advice promptly.Â
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Patient information leafletÂ
Generic Name: isoxicamÂ
Pronounced: eye-SOKS-i-kamÂ
Why do we use isoxicam?Â
Isoxicam, classified as a nonsteroidal anti-inflammatory drug (NSAID) and belonging to the oxicam class of NSAIDs, is primarily utilized for its anti-inflammatory, analgesic (pain-relieving), and antipyretic (fever-reducing) attributes. Its mechanism of action involves the inhibition of prostaglandin production, key chemicals in the body associated with inflammation, pain, and fever.Â
This medication is frequently prescribed to alleviate symptoms linked to conditions like osteoarthritis and rheumatoid arthritis. Isoxicam proves effective in diminishing pain, swelling, and joint stiffness associated with these inflammatory disorders.Â
The decision to use isoxicam should be grounded in a healthcare professional’s evaluation of the individual’s medical condition, weighing the potential benefits and risks of the drug. Adherence to the prescribed dosage and recommendations provided by the healthcare provider is crucial, and awareness of possible side effects or interactions with other medications is essential.Â