Drug profile
Piroxicam
Adult, child, renal, hepatic, pregnancy and breastfeeding information, with the source named on every line.
DRUG INFORMATION
ADULT
- For the relief of rheumatoid arthritis and osteoarthritis, the dosage is 20 mg
given orally once per day.
Source: US FDA label for piroxicam (PIROXICAM), section 'dosage and
administration', retrieved 2026-08-29
- Use the lowest effective dosage for shortest duration consistent with individual
patient treatment goals ( 2 ) OA and RA: 20 mg once daily ( 2 )
Source: US FDA label for piroxicam (PIROXICAM), section 'dosage and
administration', retrieved 2026-08-29
- Carefully consider the potential benefits and risks of piroxicam and other
treatment options before deciding to use piroxicam. Use the lowest effective
dosage for the shortest duration consistent with individual patient treatment
goals [ see Warnings and Precautions (5) ] . After observing the response to
initial therapy with piroxicam, the dose and frequency should be adjusted to suit
an individual patient’s needs.
Source: US FDA label for piroxicam (PIROXICAM), section 'dosage and
administration', retrieved 2026-08-29
CHILD
- Piroxicam has not been investigated in pediatric patients. The safety and
effectiveness of piroxicam have not been established.
Source: US FDA label for piroxicam (PIROXICAM), section 'pediatric use', retrieved
2026-08-29
RENAL IMPAIRMENT
- Consider withdrawal of piroxicam in women who have difficulties conceiving ( 8.3 )
8.1 Pregnancy Risk Summary Use of NSAIDs, including piroxicam, can cause premature
closure of the fetal ductus arteriosus and fetal renal dysfunction leading to
oligohydramnios and, in some cases, neonatal renal impairment.
Source: US FDA label for piroxicam (PIROXICAM), section 'use in specific
populations', retrieved 2026-08-29
- Oligohydramnios/Neonatal Renal Impairment Use of NSAIDs at about 20 weeks
gestation or later in pregnancy has been associated with cases of fetal renal
dysfunction leading to oligohydramnios, and in some cases, neonatal renal
impairment.
Source: US FDA label for piroxicam (PIROXICAM), section 'use in specific
populations', retrieved 2026-08-29
- Oligohydramnios/Neonatal Renal Impairment: If an NSAID is necessary at about 20
weeks gestation or later in pregnancy, limit the use to the lowest effective dose
and shortest duration possible.
Source: US FDA label for piroxicam (PIROXICAM), section 'use in specific
populations', retrieved 2026-08-29
HEPATIC IMPAIRMENT
- Discontinue if abnormal liver tests persist or worsen or if clinical signs and
symptoms of liver disease develop ( 5.3 ) Hypertension: Patients taking some
antihypertensive medications may have impaired response to these therapies when
taking NSAIDs.
Source: US FDA label for piroxicam (PIROXICAM), section 'warnings and cautions',
retrieved 2026-08-29
- Monitor blood pressure ( 5.4 , 7 ) Heart Failure and Edema: Avoid use of piroxicam
in patients with severe heart failure unless benefits are expected to outweigh
risk of worsening heart failure ( 5.5 ) Renal Toxicity: Monitor renal function in
patients with renal or hepatic impairment, heart failure, dehydration, or
hypovolemia.
Source: US FDA label for piroxicam (PIROXICAM), section 'warnings and cautions',
retrieved 2026-08-29
- Additionally, patients with advanced liver disease and/or coagulopathy are at
increased risk for GI bleeding.
Source: US FDA label for piroxicam (PIROXICAM), section 'warnings and cautions',
retrieved 2026-08-29
PREGNANCY
- Risk Summary Use of NSAIDs, including piroxicam, can cause premature closure of
the fetal ductus arteriosus and fetal renal dysfunction leading to oligohydramnios
and, in some cases, neonatal renal impairment.
Source: US FDA label for piroxicam (PIROXICAM), section 'pregnancy', retrieved
2026-08-29
- Because of these risks, limit dose and duration of piroxicam use between about 20
and 30 weeks of gestation, and avoid piroxicam use at about 30 weeks of gestation
and later in pregnancy (see Clinical Considerations, Data).
Source: US FDA label for piroxicam (PIROXICAM), section 'pregnancy', retrieved
2026-08-29
- Premature Closure of Fetal Ductus Arteriosus Use of NSAIDs, including piroxicam,
at about 30 weeks gestation or later in pregnancy increases the risk of premature
closure of the fetal ductus arteriosus.
Source: US FDA label for piroxicam (PIROXICAM), section 'pregnancy', retrieved
2026-08-29
BREASTFEEDING
- Infertility Females Based on the mechanism of action, the use of prostaglandin-
mediated NSAIDs, including piroxicam, may delay or prevent rupture of ovarian
follicles, which has been associated with reversible infertility in some women.
Source: US FDA label for piroxicam (PIROXICAM), section 'nursing mothers',
retrieved 2026-08-29
- Published animal studies have shown that administration of prostaglandin synthesis
inhibitors has the potential to disrupt prostaglandin-mediated follicular rupture
required for ovulation.
Source: US FDA label for piroxicam (PIROXICAM), section 'nursing mothers',
retrieved 2026-08-29
- Small studies in women treated with NSAIDs have also shown a reversible delay in
ovulation.
Source: US FDA label for piroxicam (PIROXICAM), section 'nursing mothers',
retrieved 2026-08-29