IN ADULTS, THE COMBINED DURATION OF USE OF KETOROLAC TROMETHAMINE INJECTION AND
KETOROLAC TROMETHAMINE TABLETS IS NOT TO EXCEED FIVE (5) DAYS. IN ADULTS, THE
USE OF KETOROLAC TROMETHAMINE TABLETS IS ONLY INDICATED AS CONTINUATION THERAPY
TO KETOROLAC TROMETHAMINE INJECTION.
Ketorolac Tromethamine Injection Adult Patients
Ketorolac Tromethamine Injection may be used as a single or multiple dose on a
regular or “prn” schedule for the management of moderately severe acute pain
that requires analgesia at the opioid level, usually in a postoperative setting.
Hypovolemia should be corrected prior to the administration of ketorolac
tromethamine. Patients should be switched to alternative analgesics as soon as
possible, but ketorolac tromethamine therapy is not to exceed five (5) days.
When administering Ketorolac Tromethamine Injection, the IV bolus must be given
over no less than 15 seconds. The IM administration should be given slowly and
deeply into the muscle. The analgesic effect begins in ~30 minutes with maximum
effect in 1 to 2 hours after dosing IV or IM. Duration of analgesic effect is
usually 4 to 6 hours.
Single-Dose Treatment: The Following Regimen Should Be Limited
to Single Administration Use Only
Adult Patients IM Dosing
Patients < 65 years of age: One dose of 60 mg.
Patients >/= 65 years of age, renally impaired and/or less than 50 kg (110 lbs)
of body weight: One dose of 30 mg.
IV Dosing
Patients < 65 years of age: One dose of 30 mg.
Patients >/= 65 years of age, renally impaired and/or less than 50 kg (110 lbs)
of body weight: One dose of 15 mg.
Multiple-Dose Treatment (IV or IM) in Adults
Patients < 65 Years of Age
The recommended dose is 30 mg Ketorolac Tromethamine Injection every 6 hours.
The maximum daily dose should not exceed 120 mg.
For Patients >/= 65 Years of Age, Renally Impaired Patients and Patients Less
Than 50 Kg (110 lbs)
The recommended dose is 15 mg Ketorolac Tromethamine Injection every 6 hours.
The maximum daily dose for these populations should not exceed 60 mg.
For breakthrough pain do not increase the dose or the frequency of ketorolac
tromethamine. Consideration should be given to supplementing these regimens with
low doses of opioids prn unless otherwise contraindicated.
Renal Dosing
See comments above.
Ketorolac tromethamine is CONTRAINDICATED in patients with advanced
renal impairment and in patients at risk for renal failure due to volume
depletion.
Ketorolac tromethamine and its metabolites are eliminated primarily by
the kidneys, which, in patients with reduced creatinine clearance, will
result in diminished clearance of the drug. Therefore, ketorolac
tromethamine should be used with caution in patients with impaired renal
function and such patients should be followed closely. With the use of
ketorolac tromethamine, there have been reports of acute renal failure,
nephritis and nephrotic syndrome.
Because patients with underlying renal insufficiency are at increased
risk of developing acute renal failure, the risks and benefits should be
assessed prior to giving ketorolac tromethamine to these patients.
Hence, in patients with moderately elevated serum creatinine, it is
recommended that the daily dose of Ketorolac Tromethamine Injection be
reduced by half, not to exceed 60 mg/day. KETOROLAC TROMETHAMINE IS
CONTRAINDICATED IN PATIENTS WITH SERUM CREATININE CONCENTRATIONS
INDICATING ADVANCED RENAL IMPAIRMENT.
Hypovolemia should be corrected before treatment with ketorolac
tromethamine is initiated.
Hemodialysis
Specific guidelines not available.
Disclaimer
The authors make no claims of the accuracy of the information contained herein; and these suggested doses are not a substitute for clinical
judgment. Neither GlobalRPh Inc. nor any other party involved in the
preparation of this program shall be liable for any special, consequential, or exemplary damages resulting in whole or part from any user's use of or reliance upon this material.PLEASE READ THE DISCLAIMER
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