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Calzim Injection

NAFDAC REG NO: A4-8733 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 6 November 2026 · synced automatically from official sources.
Produit
Calzim Injection
Numéro NAFDAC
A4-8733
Principe actif
Chlorpromazine (Chlorpromazine Hydrochloride)
Dosage
50 mg/2 mL
Forme
Injection
Conditionnement
10 x 2 mL ampoules
Fabricant
Non répertorié
Déposant / Titulaire :
Chupet Pharmaceutical Company Limited
Approuvé
22 Oct 2022
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
21 Oct 2027
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

About the medicine: Chlorpromazine: uses, dosage and brands worldwide

What we found

  • Calzim Injection is on the NAFDAC register with an active registration (A4-8733). 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 Calzim Injection

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 : Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Analyses of seventeen placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated patients of between 1.6 to 1.7 times the risk of death in placebo-treated patients. …
Pour qui

For the management of manifestations of psychotic disorders. For the treatment of schizophrenia. To control nausea and vomiting. For relief of restlessness and apprehension before surgery. For acute intermittent porphyria. As an adjunct in the treatment of tetanus. To control the manifestations of the manic type of manic-depressive illness. For relief of intractable hiccups. …

Comment le prendre et à quelle fréquence
  • ? ADULTS Adjust dosage to individual and the severity of his condition, recognizing that the milligram for milligram potency relationship among all dosage forms has not been precisely established clinically
  • It is important to increase dosage until symptoms are controlled
  • Dosage should be increased more gradually in debilitated or emaciated patients
  • In continued therapy, gradually reduce dosage to the lowest effective maintenance level, after symptoms have been controlled for a reasonable period
  • The 100 mg and 200 mg tablets are for use in severe neuropsychiatric conditions
  • Elderly Patients - In general, dosages in the lower range are sufficient for most
  • Elderly patients
  • Since they appear to be more susceptible to hypotension and neuromuscular reactions, such patients should be observed closely
  • Dosage should be tailored to the individual, response carefully monitored, and dosage adjusted accordingly
  • Dosage should be increased more gradually in elderly patients
  • Psychotic Disorders - Increase dosage gradually until symptoms are controlled
  • Maximum improvement may not be seen for weeks or even months
  • Continue optimum dosage for 2 weeks; then gradually reduce dosage to the lowest effective maintenance level
  • Daily dosage of 200 mg is not unusual
Talk to a doctor first if
  • Do not use in patients with known hypersensitivity to phenothiazines
  • Do not use in comatose states or in the presence of large amounts of central nervous system depressants (alcohol, barbiturates, narcotics, etc.)
Warnings

Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Chlorpromazine hydrochloride is not approved for the treatment of patients with dementia-related psychosis [see BOXED WARNING] . The extrapyramidal symptoms which can occur secondary to chlorpromazine may be confused with the central nervous system signs of an undiagnosed primary disease responsible for the vomiting, e.g., Reye's syndrome or other encephalopathy. …

Effets secondaires possibles

Note: Some adverse effects of chlorpromazine may be more likely to occur, or occur with greater intensity, in patients with special medical problems, e.g., patients with mitral insufficiency or pheochromocytoma have experienced severe hypotension following recommended doses. Drowsiness: Usually mild to moderate, may occur, particularly during the first or second week, after which it generally disappears. If troublesome, dosage may be lowered. Jaundice: Overall incidence has been low, regardless of indication or dosage. Most investigators conclude it is a sensitivity reaction. Most cases occur between the second and fourth weeks of therapy. …

If you take too much

[See also ADVERSE REACTIONS ] . Symptoms Primarily symptoms of central nervous system depression to the point of somnolence or coma. Hypotension and extrapyramidal symptoms. Other possible manifestations include agitation and restlessness, convulsions, fever, autonomic reactions such as dry mouth and ileus. EKG changes and cardiac arrhythmias. Treatment It is important to determine other medications taken by the patient since multiple drug therapy is common in overdosage situations. Treatment is essentially symptomatic and supportive. Early gastric lavage is helpful. …

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 2026-08-19.

Label for chlorpromazine (chlorpromazine hydrochloride), the active ingredient registered with NAFDAC.

Check your pack of Calzim Injection

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

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Encore 3 vérifications gratuites aujourd'hui Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Calzim Injection

What is in Calzim Injection?

Calzim Injection contains Chlorpromazine (Chlorpromazine Hydrochloride) (50 mg/2 mL), as injection, according to its NAFDAC registration record.

Is Calzim Injection registered with NAFDAC?

Yes. Calzim Injection is listed on the NAFDAC register under registration number A4-8733, and its registration is active as of 6 November 2026.

Has Calzim Injection been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Calzim Injection in our automatically synced alert list.

How can I check that my pack of Calzim Injection is genuine?

Run a free authenticity scan with the NAFDAC number A4-8733, 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 Calzim Injection?

Follow your prescription or the leaflet in your pack. The official label says: – ADULTS Adjust dosage to individual and the severity of his condition, recognizing that the milligram for milligram potency relationship among all dosage forms has not been precisely established clinically. It is important to increase dosage until symptoms are controlled. Dosage should be increased more gradually in debilitated or emaciated patients. In continued therapy, grad…

What is Calzim Injection used for?

For the management of manifestations of psychotic disorders. For the treatment of schizophrenia. To control nausea and vomiting. For relief of restlessness and apprehension before surgery. For acute intermittent porphyria. As an adjunct in the treatment of tetanus. To control the manifestations of the manic type of manic-depressive illness. For relief of intractable hiccups. … (Summarised from the official U.S. FDA label for chlorpromazine (chlorpromazine hydrochloride). Always follow your doctor or pharmacist.)

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