Zeropain-IM/IV 60 Injection
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Zeropain 60mg/2ml Injection

Generic: Ketorolac Tromethamine

Type: Injection

Pack Size: 2pcs

Zeropain (Ketorolac Tromethamine) is a powerful short-term analgesic for managing moderate to severe pain. Due to its side effect profile (especially GI and renal), it is typically limited to short-term use (≤5 days). Patients must be closely monitored for gastrointestinal, renal, and cardiovascular complications, particularly the elderly or those with preexisting conditions.

  • Adults:
    Recommended doses depend on the formulation and route (oral, IV, IM). Usually not exceeding 5 days of treatment due to potential toxicity.
  • Children:
    Not recommended for patients under 16 years.

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✅ Description:

Zeropain is a pyrrolo-pyrrole NSAID used for its potent analgesic (pain-relieving) properties. It functions primarily by inhibiting prostaglandin synthesis via the cyclooxygenase (COX) enzyme, leading to its pain-relief effects. However, it exhibits minimal anti-inflammatory properties at its usual analgesic doses.

  • Chemical Composition:
    5-benzoyle-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid with 2-amino-2-(hydroxymethyl)-1,3-propanediol (1:1).
Pack Image of Zeropain 60 mg Injection

Pharmacokinetics

  • Absorption: Rapidly absorbed after administration.
  • Protein Binding: Highly protein-bound.
  • Metabolism: Primarily metabolized in the liver.
  • Excretion: Excreted through urine as metabolites and some unchanged drugs.
  • Linear Pharmacokinetics: Drug levels are proportional to dose.

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✔️ Indications
  1. Acute pain management (short-term use only, typically 5 days or less).
  2. Post-surgical pain (excluding prophylactic use before surgery).
  3. Conditions requiring a non-opioid alternative for moderate to severe pain.
✔️ Side Effects

Common:

  • Gastrointestinal: Nausea, vomiting, GI bleeding, melena, peptic ulcers, pancreatitis.
  • Neurological: Anxiety, headache, drowsiness.
  • Cardiovascular: Bradycardia, hypertension, palpitation, chest pain.
  • Other: Infertility in females, pulmonary edema.

Rare but Severe:

  • Anaphylactic reactions.
  • Hepatotoxicity or renal toxicity.
✔️ Ketorolac Tromethamine Injection: Detailed Dosage and Administration
  • Ketorolac injection is used for the management of moderately severe acute pain requiring opioid-level analgesia, often in a postoperative setting.
  • Administered as IV or IM for short-term use (≤5 days) due to potential side effects.
✔️ Single-Dose Treatment

IM Dosing (Adults):

  1. Adults <65 years:
    • Dose: 60 mg IM as a single dose.
  2. Adults ≥65 years, renally impaired, or weighing <50 kg:
    • Dose: 30 mg IM as a single dose.

IV Dosing (Adults):

  1. Adults <65 years:
    • Dose: 30 mg IV as a single dose.
  2. Adults ≥65 years, renally impaired, or weighing <50 kg:
    • Dose: 15 mg IV as a single dose.
✔️ IV or IM Dosing (Children 2–16 years):
  1. IM Dosing:
    • Dose: 1 mg/kg IM, up to a maximum of 30 mg.
  2. IV Dosing:
    • Dose: 0.5 mg/kg IV, up to a maximum of 15 mg.
✔️ Multiple-Dose Treatment Adults <65 years:
  • Dose: 30 mg every 6 hours (IV or IM).
  • Maximum daily dose: 120 mg.
✔️ Adults ≥65 years, renally impaired, or weighing <50 kg:
  • Dose: 15 mg every 6 hours (IV or IM).
  • Maximum daily dose: 60 mg.
✔️ Conversion from Parenteral to Oral Therapy
  1. Oral Ketorolac tablets can replace injections when feasible.
  2. Maximum total daily dose (oral + parenteral):
    • Adults <65 years: 120 mg on the day of transition.
    • Adults ≥65 years or renally impaired: 60 mg on the day of transition.
  3. Subsequent oral dosing:
    • Max daily dose: 40 mg orally.
  4. Duration of combined treatment (parenteral + oral):
    • Should not exceed 5 days.
✔️ Administration Guidelines
  1. IV Bolus:
    • Administer over no less than 15 seconds.
  2. IM Injection:
    • Inject slowly and deeply into the muscle.
✔️ Onset, Peak Effect, and Duration
  • Onset: Begins within 30 minutes after IV or IM administration.
  • Peak Effect: Achieved in 1–2 hours.
  • Duration: Last for 4–6 hours.
✔️ Important Warnings
  1. Do not increase the dose or frequency for breakthrough pain.
  2. Ensure total treatment duration (IV, IM, and oral combined) does not exceed 5 days to minimize risks of adverse effects.
  3. Monitor patients for potential GI bleeding, renal impairment, and hypersensitivity reactions.
✔️ Mechanism of Action:

Ketorolac inhibits the COX enzyme system, which reduces prostaglandin production. This results in pain relief and reduced inflammation, although anti-inflammatory effects are less pronounced.

✔️ Drug Interactions
  1. Other NSAIDs/Aspirin: Increases risk of side effects (e.g., GI bleeding).
  2. Anticoagulants: Enhances bleeding risk.
  3. ACE Inhibitors/Beta Blockers: May reduce anti-hypertensive effects or impair kidney function.
  4. Methotrexate: Increases risk of toxicity.
✔️ Contraindications
  • Hypersensitivity to Ketorolac or any NSAID.
  • Active or suspected peptic ulcers or gastrointestinal bleeding.
  • Patients with asthma, renal impairment, or liver dysfunction.
  • Pregnancy (especially third trimester) and lactation.
  • Not to be used as a prophylactic analgesic before surgery.
✔️ Pregnancy & Lactation
  • FDA Pregnancy Category C: Avoid during pregnancy unless benefits outweigh risks. Contraindicated in the third trimester due to risk of premature ductus arteriosus closure.
  • Avoid during lactation, as Ketorolac passes into breast milk.
✔️ Precautions & Warnings
  1. Elderly patients (>65 years): Increased risk of GI and renal side effects; requires caution.
  2. Liver & Kidney Dysfunction: Monitor liver enzymes and renal function.
  3. Asthma: Risk of NSAID-exacerbated respiratory issues.
  4. Ophthalmic Use: Discontinue immediately if corneal epithelial breakdown occurs; avoid wearing contact lenses during treatment.
✔️ Storage
  • Store in a dry, cool place (<30°C), away from light and moisture.
  • Keep out of reach of children.
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