The adverse reactions listed as follows are reported as probably related to ketorolac in clinical trials: Incidence >1%: Percentage incidence was reported in ≥3% patients: Body as a Whole: Edema (4%).
Cardiovascular: Hypertension.
Dermatologic: Pruritus, rash.
Gastrointestinal: Nausea (12%), dyspepsia (12%), gastrointestinal pain (13%), diarrhea (7%), constipation, flatulence, gastrointestinal fullness, vomiting and stomatitis.
Hematologic and Lymphatic: Purpura.
Central Nervous System: Cephalgia (17%), drowsiness (6%), dizziness (7%), swelling.
Pain on injection sites was reported by 2% of patients studied with multiple doses.
Incidence ≤1%: Body as a Whole: Increased weight, fever, infections, asthenia.
Cardiovascular: Palpitations, not for cardiovascular effects.
Dermatological: Urticaria.
Gastrointestinal: Gastritis, rectal bleeding, belch, anorexia, and/or increased appetite.
Hematologic and Lymphatic: Epistaxis, anemia, eosinophilia. Nervous System: Tremor, abnormal dreams, hallucinations, euphoria, extrapyramidal symptoms, vertigo, paresthesia, depression, insomnia, nervousness, excessive thirst, dry mouth, abnormal vision, difficulty to concentrate, hyperkinesis, stupor.
Respiratory: Dyspnea, lung edema, rhinitis, cough.
Sensory: Abnormal taste, abnormal or blurred vision, tinnitus, deafness. Urogenital: Hematuria, proteinuria, oliguria, urine retention, polyuria, increased urinary frequency.
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