Ketorolac chemical structure
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Toradol


Ketorolac or ketorolac tromethamine (marketed as Toradol® - generics have been approved) is a non-steroidal anti-inflammatory drug (NSAID) in the family of propionic acids, often used as an analgesic, antipyretic (fever reducer), and anti-inflammatory. Ketorolac acts by inhibiting bodily synthesis of prostaglandins. Ketorolac in its oral and intramuscular preparations is a racemic mixture of R-(+)(which is the salt 1H-Pyrrolizine-1-carboxylic acid,5-benzoyl-2,3-dihydro- ketorolac) and S-(-) (which does not have the 1H-Pyrrolizine-1-carboxylic acid,5-benzoyl-2,3-dihydro group) ketorolac. more...

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The brand name Toradol was coined by the Syntex company of the United States.

This article does not cover Acular® or ophthalmic ketorolac.

Chemistry

Ketorolac, like other 2-arylpropionate derivatives (including ketoprofen, flurbiprofen, naproxen, ibuprofen etc.) contains a chiral carbon in the β-position of the propionate moiety. As such there are two possible enantiomers of ketorolac with the potential for different biological effects and metabolism for each enantiomer.

NSAIDs are not recommended for use with other NSAIDs because of the potential for additive side effects.

The protein-binding effect of most non-aspirin NSAIDs is inhibited by the presence of aspirin in the blood.

Mechanism of action

The primary mechanism of action responsible for Ketorolac's anti-inflammatory/antipyretic/analgesic effects is the inhibition of prostaglandin synthesis by competitive blocking of the the enzyme cyclooxygenase (COX). Like most NSAIDs, Ketorolac is a non-selective cyclooxygenase inhibitor.

As with other NSAIDs, the mechanism of the drug is associated with the chiral S form. Conversion of the R enantiomer into the S enantiomer has been shown to occur in the metabolism of ibuprofen; it is unknown whether it occurs in the metabolism of ketorolac.

Image:Ketorolac bottles.jpg

Indications

Ketorolac is indicated for short-term management of pain (up to five days).

Contraindications

Ketorolac is contraindicated against patients with a previously demonstrated hypersensitivity to ketorolac, and against patients with the complete or partial syndrome of nasal polyps, angioedema, bronchospastic reactivity or other allergic manifestations to aspirin or other non-steroidal anti-inflammatory drugs (due to possibility of severe anaphylaxis).

Adverse effects

Similar to other NSAIDs. See inset "Ketorolac adverse effects."

Warnings and precautions

The most serious risks associated with ketorolac are, as with other NSAIDs, gastrointestinal ulcerations, bleeding and perforation; renal events ranging from interstitial nephritis to complete renal failure; hemorhage, and hypersensitivity reactions.

As with other NSAIDs, fluid and solute retention and edema have been reported with ketorolac; ketorolac elevated liver protein levels; it also inhibits platelet aggregation and may be associated with an increased risk of bleeding.

Notes

Ketorolac is not recommended for pre-operative analgesia or co-administration with anesthesia because it inhibits platelet aggregation.

Ketorolac is not recommended for obstetric analgesia because it has not been adequately tested for obstetrical administration and has demonstrable fetal toxicity in laboratory animals.

Read more at Wikipedia.org


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Toradol cult narcotics, pain after cesareans - Double-Blind, Randomized Study
From OB/GYN News, 5/15/03 by Betsy Bates

ANAHEIM, CALIF. -- Post-operative pain and narcotic use were significantly reduced in patients who received ketorolac tromethamine following cesarean section in a placebo-controlled, double-blind randomized study.

Starting 1 hour after administration and continuing through 24 hours, 23 patients receiving the nonsteroidal anti-inflammatory drug rated their pain at least one digit lower on a 0-10 visual analogue scale than did 22 patients receiving placebo, Dr. Jerry Lowder said at the annual meeting of the Society of Gynecologic Surgeons.

Additionally, they used a total of 28 mg of morphine from patient-controlled analgesic pumps, compared with the 42 mg used by patients who received placebo. Ketorolac tromethamine patients attempted to get more morphine 40 times during the 24-hour study period; patients receiving placebo pushed the button an average of 60 times.

Because the drug, marketed as Toradol, carries a black box warning against its use in labor and delivery, an investigational new drug application was filed and approved by the Food and Drug Administration before the study began.

Ketorolac tromethamine is widely used in gynecologic and other forms of surgery but has been contraindicated in labor, delivery, and postpartum care over concern that it could adversely affect fetal circulation and inhibit uterine contractions.

It is thought to be a potentially useful drug following cesarean section, however, because it is the only NSAID that can be administered parenterally and it has been shown to decrease pain associated with uterine contractions and surgical incisions, said Dr. Lowder of East Carolina University in Greenville, N.C.

He added that study investigators were not permitted to enroll subjects who intended to breast-feed because of the potential adverse effects of prostaglandins on neonates, even though the American Academy of Pediatrics has stated that the drug is compatible with breast-feeding.

Ketorolac tromethamine inhibits platelet function, but no increase in postoperative bleeding was seen in the study, which was cut short when an interim analysis showed such a magnitude of effect it was not considered necessary to continue enrollment to complete the intended 90-patient cohort, he said.

Dr. Lowder's coinvestigator in the study was Dr. Todd Beste, who is also with East Carolina University.

COPYRIGHT 2003 International Medical News Group
COPYRIGHT 2003 Gale Group

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