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Dolac-30 Injection## (pack size)

NAFDAC REG NO: A4-2742 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 6 November 2026 · synced automatically from official sources.
Produit
Dolac-30 Injection## (pack size)
Numéro NAFDAC
A4-2742
Principe actif
Ketorolac Tromethamine
Dosage
30 mg
Forme
Injection
Conditionnement
10 x 1 mL
Fabricant
Non répertorié
Déposant / Titulaire :
Interpharma Industries Limited
Approuvé
28 Sep 2021
Statut
Inactive Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
27 Sep 2026
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

About the medicine: Ketorolac tromethamine: uses, dosage and brands worldwide

What we found

  • Dolac-30 Injection## (pack size) is on the NAFDAC register with an active registration (A4-2742). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Dolac-30 Injection## (pack size)

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Mise en garde grave : Ketorolac tromethamine, a nonsteroidal anti-inflammatory drug (NSAID), is indicated for the short-term (up to 5 days in adults) management of moderately severe acute pain that requires analgesia at the opioid level. Oral ketorolac tromethamine is indicated only as continuation treatment following intravenous or intramuscular dosing of ketorolac tromethamine, if necessary. …
Pour qui

Carefully consider the potential benefits and risks of ketorolac tromethamine and other treatment options before deciding to use ketorolac. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Acute Pain in Adult Patients Ketorolac tromethamine is indicated for the short-term (≤5 days) management of moderately severe acute pain that requires analgesia at the opioid level, usually in a postoperative setting. Therapy should always be initiated with intravenous or intramuscular dosing of ketorolac tromethamine, and oral ketorolac tromethamine is to be used only as continuation treatment, if necessary. …

Comment le prendre et à quelle fréquence
  • Carefully consider the potential benefits and risks of ketorolac tromethamine and other treatment options before deciding to use ketorolac tromethamine
  • Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals
  • In adults, the combined duration of use of intravenous or intramuscular dosing of ketorolac tromethamine and oral ketorolac tromethamine is not to exceed 5 days
  • In adults, the use of oral ketorolac tromethamine is only indicated as continuation therapy to intravenous or intramuscular dosing of ketorolac tromethamine
  • See package insert for ketorolac tromethamine tablets for transition from intravenous or intramuscular dosing of ketorolac tromethamine (single- or multiple-dose) to multiple-dose oral ketorolac tromethamine
  • Note: Oral formulation should not be given as an initial dose
  • Use minimum effective dose for the individual patient
  • Total duration of treatment in adult patients: the combined duration of use of intravenous or intramuscular dosing of ketorolac tromethamine and oral ketorolac tromethamine is not to exceed 5 days
  • KETOROLAC TROMETHAMINE INJECTION 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 (see WARNINGS – Renal Effects ). …
Talk to a doctor first if
  • (see also Boxed WARNING ) Ketorolac Tromethamine is contraindicated in patients with previously demonstrated hypersensitivity to ketorolac tromethamine
  • Ketorolac tromethamine is contraindicated in patients with active peptic ulcer disease, in patients with recent gastrointestinal bleeding or perforation and in patients with a history of peptic ulcer disease or gastrointestinal bleeding. …
Warnings

(See also Boxed WARNING .) The total combined duration of use of oral ketorolac tromethamine and intravenous or intramuscular dosing of ketorolac tromethamine is not to exceed 5 days in adults. Ketorolac tromethamine is not indicated for use in pediatric patients. The most serious risks associated with ketorolac tromethamine are: Gastrointestinal Effects – Risk of Ulceration, Bleeding and Perforation: Ketorolac tromethamine is contraindicated in patients with previously documented peptic ulcers and/or gastrointestinal (GI) bleeding. …

Effets secondaires possibles

Adverse reaction rates increase with higher doses of ketorolac tromethamine. Practitioners should be alert for the severe complications of treatment with ketorolac tromethamine, such as G.I. ulceration, bleeding and perforation, postoperative bleeding, acute renal failure, anaphylactic and anaphylactoid reactions and liver failure (see Boxed WARNING , WARNINGS , PRECAUTIONS , and DOSAGE AND ADMINISTRATION ). These NSAID-related complications can be serious in certain patients for whom ketorolac tromethamine is indicated, especially when the drug is used inappropriately. …

If you take too much

Symptoms and Signs Symptoms following acute NSAIDs overdoses are usually limited to lethargy, drowsiness, nausea, vomiting, and epigastric pain, which are generally reversible with supportive care. Gastrointestinal bleeding can occur. Hypertension, acute renal failure, respiratory depression and coma may occur, but are rare. Anaphylactoid reactions have been reported with therapeutic ingestion of NSAIDs, and may occur following an overdose. Treatment Patients should be managed by symptomatic and supportive care following a NSAIDs overdose. There are no specific antidotes. …

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2022-10-12.

Label for ketorolac tromethamine, the active ingredient registered with NAFDAC.

Check your pack of Dolac-30 Injection## (pack size)

Add the expiry date on your pack for a full Trust Score.

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About Dolac-30 Injection## (pack size)

What is in Dolac-30 Injection## (pack size)?

Dolac-30 Injection## (pack size) contains Ketorolac Tromethamine (30 mg), as injection, according to its NAFDAC registration record.

Is Dolac-30 Injection## (pack size) registered with NAFDAC?

Yes. Dolac-30 Injection## (pack size) is listed on the NAFDAC register under registration number A4-2742, and its registration is active as of 6 November 2026.

Has Dolac-30 Injection## (pack size) been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Dolac-30 Injection## (pack size) in our automatically synced alert list.

How can I check that my pack of Dolac-30 Injection## (pack size) is genuine?

Run a free authenticity scan with the NAFDAC number A4-2742, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take Dolac-30 Injection## (pack size)?

Follow your prescription or the leaflet in your pack. The official label says: Carefully consider the potential benefits and risks of ketorolac tromethamine and other treatment options before deciding to use ketorolac tromethamine. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals. In adults, the combined duration of use of intravenous or intramuscular dosing of ketorolac tromethamine and oral ketor…

What is Dolac-30 Injection## (pack size) used for?

Carefully consider the potential benefits and risks of ketorolac tromethamine and other treatment options before deciding to use ketorolac. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Acute Pain in Adult Patients Ketorolac tromethamine is indicated for the short-term (≤5 days) management of moderately severe acute pain (Summarised from the official U.S. FDA label for ketorolac tromethamine. Always follow your doctor or pharmacist.)

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