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Zuresi Diazepam 10 mg

NAFDAC Reg. No. A11-100912 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Controlled medicine: DiazepamPrescription only. A licensed pharmacist may sell it only against a doctor's prescription.

Diazepam · Benzodiazepine (sedative) · UN 1971 Schedule IV

  • Dependence after a few weeks of daily use; do not stop suddenly
  • Drowsiness, falls and road accidents
  • Dangerous with alcohol or opioid painkillers: breathing can stop
Product
Zuresi Diazepam 10 mg
NAFDAC number
A11-100912
Active ingredient
Diazepam
Strength
10 mg
Form
Tablet
Pack size
1 x 100's (in jar)
Manufacturer
Not listed
Applicant (holder)
VCA American Pharmaceuticals Ltd
Approved
25 Jun 2025
Status
Active View on NAFDAC ↗
Registration valid to
24 Jun 2030
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Zuresi Diazepam 10 mg is on the NAFDAC register with an active registration (A11-100912). 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 Zuresi Diazepam 10 mg

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Serious warning: RISKS FROM CONCOMITANT USE WITH OPIOIDS; ABUSE, MISUSE, AND ADDICTION; and DEPENDENCE AND WITHDRAWAL REACTIONS • Concomitant use of benzodiazepines and opioids may result in profound sedation, respiratory depression, coma, and death. Reserve concomitant prescribing of these drugs in patients for whom alternative treatment options are inadequate. Limit dosages and durations to the minimum required. …
Who it is for

Diazepam tablets are indicated for the management of anxiety disorders or for the short-term relief of the symptoms of anxiety. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic. In acute alcohol withdrawal, diazepam tablets may be useful in the symptomatic relief of acute agitation, tremor, impending or acute delirium tremens and hallucinosis. …

How to take it and how often
  • Dosage should be individualized for maximum beneficial effect
  • While the usual daily dosages given below will meet the needs of most patients, there will be some who may require higher doses
  • In such cases dosage should be increased cautiously to avoid adverse effects
  • ADULTS: USUAL DAILY DOSE: Management of Anxiety Disorders and Relief of Symptoms of Anxiety
  • Depending upon severity of symptoms—2 mg to 10 mg, 2 to 4 times daily Symptomatic Relief in Acute Alcohol Withdrawal. 10 mg, 3 or 4 times during the first 24 hours, reducing to 5 mg, 3 or 4 times daily as needed
  • Adjunctively for Relief of Skeletal Muscle Spasm. 2 mg to 10 mg, 3 or 4 times daily Adjunctively in Convulsive Disorders. 2 mg to 10 mg, 2 to 4 times daily Geriatric Patients, or in the presence of debilitating disease. 2 mg to 2.5 mg, 1 or 2 times daily initially; increase gradually as needed and tolerated
  • PEDIATRIC PATIENTS: Because of varied responses to CNS-acting drugs, initiate therapy with lowest dose and increase as required
  • Not for use
  • Pediatric patients under 6 months. 1 mg to 2.5 mg, 3 or 4 times daily initially; increase gradually as needed and tolerated
  • Discontinuation or Dosage Reduction of Diazepam Tablets To reduce the risk of withdrawal reactions, use a gradual taper to discontinue diazepam tablets or reduce the dosage
  • If a patient develops withdrawal reactions, consider pausing the taper or increasing the dosage to the previous tapered dosage level. …
Children
  • Safety and effectiveness
  • Pediatric patients below the age of 6 months have not been established
Older adults

In elderly patients, it is recommended that the dosage be limited to the smallest effective amount to preclude the development of ataxia or oversedation (2 mg to 2.5 mg once or twice daily, initially to be increased gradually as needed and tolerated). Extensive accumulation of diazepam and its major metabolite, desmethyldiazepam, has been noted following chronic administration of diazepam in healthy elderly male subjects. …

While you are taking it
  • Advise the patient to read the FDA-approved patient labeling ( Medication Guide )
  • Risks from Concomitant Use with Opioids Advise both patients and caregivers about the risks of potentially fatal respiratory depression and sedation when diazepam tablets are used with opioids and not to use such drugs concomitantly unless supervised by a health care provider
  • Advise patients not to drive or operate heavy machinery until the effects of concomitant use with the opioid have been determined (see WARNINGS: Risks from Concomitant Use with Opioids and PRECAUTIONS: Drug Interactions ). …
Talk to a doctor first if
  • Diazepam tablets are contraindicated in patients with a known hypersensitivity to diazepam and, because of lack of sufficient clinical experience, in
  • Pediatric patients under 6 months of age
  • Diazepam tablets are also contraindicated in patients with myasthenia gravis, severe respiratory insufficiency, severe hepatic insufficiency, and sleep apnea syndrome. …
Medicines it may not mix with

Opioids The concomitant use of benzodiazepines and opioids increases the risk of respiratory depression because of actions at different receptor sites in the CNS that control respiration. Benzodiazepines interact at GABA A sites and opioids interact primarily at mu receptors. When benzodiazepines and opioids are combined, the potential for benzodiazepines to significantly worsen opioid-related respiratory depression exists. Limit dosage and duration of concomitant use of benzodiazepines and opioids, and monitor patients closely for respiratory depression and sedation. …

Warnings

Risks from Concomitant Use with Opioids Concomitant use of benzodiazepiones, including diazepam tablets, and opioids may result in profound sedation, respiratory depression, coma, and death. Because of these risks, reserve concomitant prescribing of these drugs in patients for whom alternative treatment options are inadequate. Observational studies have demonstrated that concomitant use of opioid analgesics and benzodiazepines increases the risk of drug-related mortality compared to use of opioids alone. …

Possible side effects

Side effects most commonly reported were drowsiness, fatigue, muscle weakness, and ataxia. The following have also been reported: Central Nervous System: confusion, depression, dysarthria, headache, slurred speech, tremor, vertigo Gastrointestinal System: constipation, nausea, gastrointestinal disturbances Special Senses: blurred vision, diplopia, dizziness Cardiovascular System: hypotension Psychiatric and Paradoxical Reactions: stimulation, restlessness, acute hyperexcited states, anxiety, agitation, aggressiveness, irritability, rage, hallucinations, psychoses, delusions, increased muscle spasticity, insomnia, sleep disturbances, and nightmares. …

Pregnancy and breastfeeding

Neonatal Sedation and Withdrawal Syndrome Use of diazepam tablets late in pregnancy can result in sedation (respiratory depression, lethargy, hypotonia) and/or withdrawal symptoms (hyperreflexia, irritability, restlessness, tremors, inconsolable crying, and feeding difficulties) in the neonate (see PRECAUTIONS: Pregnancy ). …

If you take too much

Overdosage of benzodiazepines is characterized by central nervous system depression ranging from drowsiness to coma. In mild to moderate cases, symptoms can include drowsiness, confusion, dysarthria, lethargy, hypnotic state, diminished reflexes, ataxia, and hypotonia. Rarely, paradoxical or disinhibitory reactions (including agitation, irritability, impulsivity, violent behavior, confusion, restlessness, excitement, and talkativeness) may occur. In severe overdosage cases, patients may develop respiratory depression and coma. …

Dependence and misuse

Controlled Substance Diazepam tablets contain diazepam, a Schedule IV controlled substance. Abuse Diazepam tablets are a benzodiazepine and a CNS depressant with a potential for abuse and addiction. Abuse is the intentional, non-therapeutic use of a drug, even once, for its desirable psychological or physiological effects. …

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

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 2025-10-27.

Label for diazepam, the active ingredient registered with NAFDAC.

Check your pack of Zuresi Diazepam 10 mg

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

3 free checks left today Official sources: NAFDAC · WHO · U.S. FDA · Health Canada · NLM

About Zuresi Diazepam 10 mg

What is in Zuresi Diazepam 10 mg?

Zuresi Diazepam 10 mg contains Diazepam (10 mg), as tablet, according to its NAFDAC registration record.

Is Zuresi Diazepam 10 mg registered with NAFDAC?

Yes. Zuresi Diazepam 10 mg is listed on the NAFDAC register under registration number A11-100912, and its registration is active as of 28 October 2026.

Has Zuresi Diazepam 10 mg been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Zuresi Diazepam 10 mg in our automatically synced alert list.

How can I check that my pack of Zuresi Diazepam 10 mg is genuine?

Run a free authenticity scan with the NAFDAC number A11-100912, 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.

Do I need a prescription for Zuresi Diazepam 10 mg?

Yes. Zuresi Diazepam 10 mg contains diazepam, a controlled medicine. Prescription only. A licensed pharmacist may sell it only against a doctor's prescription.

How do I take Zuresi Diazepam 10 mg?

Follow your prescription or the leaflet in your pack. The official label says: Dosage should be individualized for maximum beneficial effect. While the usual daily dosages given below will meet the needs of most patients, there will be some who may require higher doses. In such cases dosage should be increased cautiously to avoid adverse effects. ADULTS: USUAL DAILY DOSE: Management of Anxiety Disorders and Relief of Symptoms of Anxiety. Depending upon se…

What is Zuresi Diazepam 10 mg used for?

Diazepam tablets are indicated for the management of anxiety disorders or for the short-term relief of the symptoms of anxiety. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic. In acute alcohol withdrawal, diazepam tablets may be useful in the symptomatic relief of acute agitation, tremor, impending or acute delirium tremens and (Summarised from the official U.S. FDA label for diazepam. Always follow your doctor or pharmacist.)

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