Toradol is a prescription nonsteroidal anti‑inflammatory drug (NSAID) used for short‑term treatment of moderately severe acute pain, often after surgery. It works by blocking prostaglandins that drive pain and inflammation. Because Toradol carries important risks—including stomach and intestinal bleeding, kidney problems, and rare cardiovascular events—it is intended for the lowest effective dose and a maximum combined duration of five days for injection and tablets. It is not an opioid and does not treat chronic pain. Always use under medical supervision and tell your clinician about other medicines, allergies, and your health history before starting ketorolac or pregnancy status.
Toradol is an NSAID analgesic indicated for the short‑term management of moderately severe acute pain that typically requires analgesia at the opioid level, such as post‑operative pain, acute musculoskeletal injuries, renal colic, or acute dental pain. Unlike opioids, ketorolac does not cause physical dependence or respiratory depression, but it also does not treat chronic or neuropathic pain and is not appropriate for long‑term use. It can reduce the need for opioids in the immediate post‑operative period as part of a multimodal pain plan. Toradol is available in injectable (IV/IM), oral tablet, and intranasal forms; ophthalmic ketorolac exists but is a different product for eye inflammation.
A defining feature of Toradol is its strict five‑day total therapy limit for systemic use (injections plus tablets combined). This cap reflects the known risk of dose‑ and duration‑dependent adverse effects, especially gastrointestinal ulceration and bleeding and kidney injury. Patients with low cardiovascular and gastrointestinal risk who need brief, strong non‑opioid pain control may benefit most. Clinicians often initiate with IV or IM ketorolac in hospital or clinic settings, then transition to oral dosing to complete the short course if needed. Always discuss your medical history and bleeding, kidney, and heart risk factors before starting ketorolac.
Dosing must be individualized, using the lowest effective dose for the shortest time, and never exceeding five total days of systemic therapy. Adults under 65 years with normal renal function: typical single IV dose is 30 mg (or 60 mg IM), or 15–30 mg IV/IM every 6 hours as needed, not to exceed 120 mg/day. For adults age 65 and older, those under 50 kg (110 lb), or those with renal impairment: use 15 mg IV/IM every 6 hours as needed, with a maximum of 60 mg/day. Oral ketorolac is generally used only as continuation after parenteral dosing: 10 mg initially, then 10 mg every 4–6 hours as needed, not exceeding 40 mg/day.
Intranasal ketorolac (Sprix) may be used short‑term for moderate to moderately severe pain when injections are impractical. Adults under 65 years typically use 31.5 mg (one spray in each nostril) every 6–8 hours, not exceeding 126 mg/day. For those 65 and older or with renal impairment, the dose is 15.75 mg every 6–8 hours, not exceeding 63 mg/day. Regardless of route, total duration must not exceed five days. Take oral tablets with food or milk to reduce stomach upset, and never combine with other NSAIDs (including ibuprofen, naproxen, or high‑dose aspirin) while on ketorolac.
Toradol carries boxed warnings for serious gastrointestinal (GI) bleeding, ulcer, and perforation; cardiovascular thrombotic events (heart attack, stroke); and renal toxicity. Risk rises with dose and duration, in older adults, with prior peptic ulcer or GI bleed, concurrent anticoagulants, steroids, SSRIs/SNRIs, heavy alcohol use, smoking, or H. pylori infection. Avoid ketorolac after coronary artery bypass graft (CABG) surgery. It inhibits platelet function and may increase bleeding, so caution is critical around surgery and in patients with bleeding disorders. NSAIDs can cause fluid retention, worsen hypertension, and precipitate kidney injury, particularly in dehydrated patients or those on ACE inhibitors/ARBs and diuretics. Report black/tarry stools, vomiting blood, chest pain, shortness of breath, sudden weakness, severe abdominal pain, decreased urine, swelling, or rash immediately.
Do not use ketorolac in patients with active peptic ulcer disease, recent GI bleeding or perforation, history of NSAID‑related GI bleeding/ulcer, advanced renal impairment or risk of renal failure due to volume depletion, hemorrhagic diathesis, suspected or confirmed cerebrovascular bleeding, or high bleeding risk. Ketorolac is contraindicated during labor and delivery (risk of fetal circulation compromise), and should be avoided from 20 weeks’ gestation onward due to fetal renal dysfunction and oligohydramnios; it is contraindicated in the third trimester. Do not administer intrathecally or epidurally. Concomitant use with other NSAIDs or aspirin at analgesic doses, probenecid, or pentoxifylline is contraindicated. Use in pediatrics is limited; oral ketorolac is not approved for children.
Common adverse effects include nausea, dyspepsia, abdominal pain, diarrhea, headache, dizziness, drowsiness, edema, sweating, and injection‑site pain. Less common but serious reactions include GI ulceration, bleeding, or perforation; renal injury (reduced urine, elevated creatinine, swelling, hyperkalemia); hepatotoxicity (elevated liver enzymes, jaundice); severe skin reactions (Stevens‑Johnson syndrome, toxic epidermal necrolysis); anaphylaxis or bronchospasm (especially with aspirin‑exacerbated respiratory disease); hypertension, heart failure exacerbation, and thrombotic cardiovascular events; and postoperative bleeding. Stop the medication and seek urgent care for black stools, vomiting blood, severe or persistent stomach pain, chest pain, sudden weakness or slurred speech, trouble breathing, facial or throat swelling, hives, peeling rash, markedly decreased urination, or yellowing of the skin or eyes.
Avoid using Toradol with other NSAIDs (ibuprofen, naproxen, diclofenac) or high‑dose aspirin due to additive GI and renal toxicity. Combining with anticoagulants (warfarin, heparin), antiplatelets (clopidogrel), SSRIs/SNRIs, or systemic corticosteroids heightens bleeding risk. ACE inhibitors/ARBs and diuretics can interact to impair renal perfusion (“triple whammy”), increasing acute kidney injury risk—ensure hydration and monitoring. Probenecid and pentoxifylline are contraindicated. Ketorolac may raise lithium levels and increase methotrexate toxicity; monitor or avoid. Calcineurin inhibitors (cyclosporine, tacrolimus) carry additive nephrotoxicity. Alcohol raises GI bleeding risk. Always provide a complete medication and supplement list—especially blood thinners, mood medications, migraine drugs, and over‑the‑counter pain relievers—so your clinician can prevent harmful combinations.
Toradol is typically taken on an as‑needed schedule within prescribed intervals. If you are on a scheduled regimen and miss a dose, take it when you remember unless it is close to the next dose—then skip the missed dose and resume your usual timing. Do not double up. Respect minimum intervals (every 4–6 hours for oral, every 6 hours for IV/IM or intranasal) and never exceed the daily maximums or the five‑day total duration. If pain persists or worsens, contact your clinician rather than self‑increasing the dose.
Ketorolac overdose may present with severe stomach pain, nausea, vomiting, drowsiness, dizziness, black or bloody stools, vomiting blood, kidney problems (reduced urine, swelling), high potassium, low blood pressure, breathing difficulties, or coma. Serious GI bleeding and acute kidney failure are medical emergencies. If an overdose is suspected, call your local emergency number or Poison Control (in the U.S., 1‑800‑222‑1222) immediately. Do not induce vomiting unless instructed by medical professionals. Bring the medication container and any co‑ingested substances to the emergency department to assist treatment.
Store Toradol tablets and injectable vials at controlled room temperature (68–77°F or 20–25°C), protected from light and moisture, and keep in the original container with the label intact. Do not freeze injectable solutions. Intranasal products should be stored and used per the package insert, with attention to discard timelines after opening. Keep all medications out of reach of children and pets. Properly dispose of expired or unused NSAIDs; for injectables, use a sharps container for needles and follow local guidelines or pharmacy take‑back programs for safe disposal.
In the United States, Toradol (ketorolac) is a prescription‑only medicine. Buying or using ketorolac without a valid prescription is not legal and can be dangerous. We cannot assist with obtaining Toradol without a prescription. The safe, lawful path is to be evaluated by a licensed clinician who can determine whether ketorolac is appropriate and, if so, prescribe it within the FDA‑mandated limits. HealthSouth Hospital of Altamonte Springs supports a legal and structured process by connecting patients with compliant telehealth consultations and coordinating dispensing after a clinician issues a valid prescription. This approach preserves safety, verifies medical necessity, and ensures you receive authentic medication and proper counseling.
Toradol is a prescription NSAID for short-term treatment of moderate to severe acute pain, often after surgery, injury, or in the emergency department.
It blocks cyclooxygenase (COX) enzymes to reduce prostaglandins, decreasing pain and inflammation without being an opioid.
IM/IV Toradol often begins working within 30–60 minutes and oral within about an hour; relief typically lasts 4–6 hours.
Total therapy should not exceed 5 days because longer use greatly increases risks of stomach bleeding, kidney injury, and other complications.
Yes, ketorolac is available as injection (IV/IM), oral tablets, and sometimes nasal spray; oral therapy usually follows initial injection.
Upset stomach, heartburn, nausea, dizziness, drowsiness, and headache are common; taking it with food can lessen stomach upset.
Serious GI bleeding/ulcer, kidney injury, increased risk of heart attack or stroke, and bleeding risk; it’s contraindicated around certain surgeries and in high-risk patients.
People with active ulcers or GI bleeding, severe kidney disease, recent or planned CABG surgery, NSAID/aspirin allergy, bleeding disorders, or in late pregnancy should avoid it.
No, do not combine Toradol with other NSAIDs (ibuprofen, naproxen, aspirin at analgesic doses) due to high bleeding and kidney risk; acetaminophen may be allowed if your clinician approves.
Avoid alcohol because it significantly increases the risk of stomach bleeding and irritation.
It can; Toradol can reduce kidney blood flow and damage the stomach lining, with risk rising in older adults, dehydrated patients, and those with prior GI or kidney issues.
Avoid in the third trimester due to fetal risks; earlier use requires specialist guidance. Small amounts may pass into breast milk—ask your clinician before use.
Yes—blood thinners (warfarin, DOACs), SSRIs/SNRIs, corticosteroids, ACE inhibitors/ARBs, diuretics, lithium, and methotrexate can interact; provide your full med list to your clinician.
No, Toradol is a non-opioid NSAID and is not addictive, but it carries significant non-addiction risks, especially with prolonged use.
It’s used for short-term acute pain to reduce opioid needs; clinicians weigh bleeding risk, kidney function, and surgical factors before using it.
It’s often used in clinics/ERs as an injection for acute migraine relief; it’s not for daily prevention and still carries GI/renal risks.
It can be effective short-term if prescribed, but dentists consider bleeding risk; never combine with other NSAIDs unless specifically instructed.
Disclose GI/ulcer history, kidney or heart disease, high blood pressure, asthma, bleeding issues, pregnancy status, alcohol use, and all medications/supplements.
Use the shortest duration prescribed; there’s no withdrawal like opioids, but stopping early may let pain return—follow your clinician’s plan.
Black or bloody stools, vomiting blood, severe stomach pain, chest pain, shortness of breath, sudden weakness, little or no urine, or a severe allergic reaction need immediate care.
Toradol is generally more potent and used for short-term moderate to severe pain, often by injection; ibuprofen is milder, OTC, and better suited to common mild to moderate pain.
Toradol offers stronger short-term relief with higher GI/renal risk and a 5-day limit; naproxen lasts longer per dose and is used for ongoing conditions but is not as potent acutely.
Toradol is preferred for brief, acute moderate to severe pain (often post-op); diclofenac is used more for chronic musculoskeletal and arthritis pain and has topical options.
Both are strong NSAIDs; indomethacin has more CNS side effects (dizziness, headache) and is used for gout and specific conditions, while Toradol has a strict 5-day limit due to GI/renal risk.
Toradol is for short bursts of acute pain; meloxicam is once-daily and better tolerated for chronic arthritis. Meloxicam is not a substitute for Toradol’s rapid, potent acute relief.
Toradol carries higher GI bleeding risk and is for short-term use; celecoxib is COX-2 selective with lower GI risk but potential cardiovascular risk, used for chronic conditions.
Avoid combining; both increase bleeding. Aspirin irreversibly inhibits platelets for heart protection, while Toradol reversibly impairs platelets and raises GI bleed risk.
Toradol is typically stronger and used briefly for moderate to severe acute pain; ketoprofen is used for mild to moderate pain and inflammation with less stringent duration limits.
Piroxicam has a very long half-life and higher ulcer risk with chronic use; Toradol is short-term only with high GI/renal risk if overused—neither suits prolonged high-dose therapy without close monitoring.
Etodolac may be somewhat COX-2–preferential and used for chronic arthritis; Toradol is more potent for acute pain but less tolerable long term, hence the 5-day cap.
Toradol injection typically starts faster and provides stronger acute relief than oral NSAIDs; it’s reserved for short-term use under medical supervision.
For routine dental pain, ibuprofen is often first choice due to safety and OTC access; Toradol may be used short-term when stronger, supervised analgesia is needed and bleeding risk is acceptable.
Toradol can rapidly reduce severe flares but is limited to brief courses; naproxen suits ongoing back pain management when an NSAID is appropriate.
Topical diclofenac targets local soft-tissue or joint pain with fewer systemic risks; Toradol treats systemic acute pain but carries higher GI/renal risks and time limits.
Meloxicam is favored for chronic arthritis due to once-daily dosing and tolerability; Toradol is not intended for chronic arthritis management.