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Aqeud 10 Tablets

NAFDAC Reg. No. B4-6029 · Drug

Registered with NAFDAC. Registration activeAs of 1 November 2026 · synced automatically from official sources.
Product
Aqeud 10 Tablets
NAFDAC number
B4-6029
Active ingredient
Aripiprazole
Strength
10 mg
Form
Tablet
Pack size
3 x 10's (in Alu-Alu blisters)
Manufacturer
Not listed
Applicant (holder)
Leotetra Healthcare Ltd
Approved
31 Jan 2024
Status
Active View on NAFDAC ↗
Registration valid to
30 Jan 2029
WHO alerts
None found
Community reports
None
Times checked
0

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

What we found

  • Aqeud 10 Tablets is on the NAFDAC register with an active registration (B4-6029). 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 Aqeud 10 Tablets

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: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS AND SUICIDAL THOUGHTS AND BEHAVIOURS WITH ANTIDEPRESSANT DRUGS Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Aripiprazole is not approved for the treatment of patients with dementia-related psychosis [see Warnings and Precautions (5.1)]. …
Who it is for

Aripiprazole is indicated for the treatment of: • Schizophrenia • Irritability Associated with Autistic Disorder • Treatment of Tourette’s Disorder Aripiprazole is an atypical antipsychotic. The oral formulations are indicated for: • Schizophrenia (14.1) • Irritability Associated with Autistic Disorder (14.4) • Treatment of Tourette’s disorder (14.5)

How to take it and how often

Initial Dose Recommended Dose Maximum Dose Schizophrenia – adults (2.1) 10 to 15 mg/day 10 to 15 mg/day 30 mg/day Schizophrenia – adolescents (2.1) 2 mg/day 10 mg/day 30 mg/day Irritability associated with autistic disorder – pediatric patients (2.4) 2 mg/day 5 to 10 mg/day 15 mg/day Tourette’s disorder – (2.5) Patients

Strengths it comes in

Aripiprazole Tablets, USP are available as described in Table 3. Table 3: Aripiprazole Tablet, USP Presentations Tablet Strength Tablet Color/Shape Tablet Markings 2 mg Off white to cream modified rectangle “251” 5 mg Off-white to light pink modified rectangle “250” 10 mg White to off white modified rectangle “252” 15 mg White to off white round “253” 20 mg White to off white round “L254” 30 mg Wh …

Children
  • The pharmacokinetics of aripiprazole and dehydro-aripiprazole
  • In pediatric patients, 10 to 17 years of age, were similar to those
  • In adults after correcting for the differences in body weight [see Clinical Pharmacology ]
  • Schizophrenia Safety and effectiveness
  • In pediatric patients with schizophrenia were established in a 6 week, placebo-controlled clinical trial in 202
  • Pediatric patients aged 13 to 17 years [see Dosage and Administration , Adverse Reactions , and Clinical Studies ]. …
Older adults

No dosage adjustment is recommended for elderly patients [see Boxed Warning, Warnings and Precautions (5.1), and Clinical Pharmacology (12.3)] . Of the 13,543 patients treated with oral aripiprazole in clinical trials, 1,073 (8%) were ≥65 years old and 799 (6%) were ≥75 years old. …

While you are taking it
  • Advise the patient to read the FDA-approved patient labeling ( Medication Guide)
  • Discuss the following issues with patients prescribed Aripiprazole: Clinical Worsening of Depression and Suicide Risk Patients, their families, and caregivers should be encouraged to be alert to the emergence of anxiety, agitation, panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity, akathisia (psychomotor restlessness), hypomania, mania, other unusual changes in behavior, worsening of depression, and suicidal ideation, especially early during antidepressant treatment and when the dose is adjusted up or down. …
Talk to a doctor first if
  • Aripiprazole is contraindicated in patients with a history of a hypersensitivity reaction to aripiprazole
  • Reactions have ranged from pruritus/urticaria to anaphylaxis [see Adverse Reactions ]. • Known hypersensitivity to aripiprazole
Medicines it may not mix with

Dosage adjustment due to drug interactions (7.1): Factors Dosage Adjustments for Aripiprazole Known CYP2D6 Poor Metabolizers Administer half of usual dose Known CYP2D6 Poor Metabolizers and strong CYP3A4 inhibitors Administer a quarter of usual dose Strong CYP2D6 or CYP3A4 inhibitors Administer half of usual dose Strong CYP2D6 and CYP3A4 inhibitors Administer a quarter of usual dose Strong CYP3A4 inducers Double usual dose over 1 to 2 weeks 7.1 Drugs Having Clinically Important Interactions with Aripiprazole Table 25: Clinically Important Drug Interactions with Aripiprazole: Concomitant Drug Name or Drug Class Clinical Rationale Clinical Recommendation Strong CYP3A4 Inhibitors (e.g., itracon …

Warnings

• Cerebrovascular Adverse Reactions in Elderly Patients with Dementia-Related Psychosis: Increased incidence of cerebrovascular adverse reactions (e.g., stroke, transient ischemic attack, including fatalities) (5.2) • Neuroleptic Malignant Syndrome: Manage with immediate discontinuation and close monitoring (5.4) • Tardive Dyskinesia: Discontinue if clinically appropriate (5.5) • Metabolic Changes: Atypical antipsychotic drugs have been associated with metabolic changes that include hyperglycemia/diabetes mellitus, dyslipidemia, and body weight gain (5.6) o Hyperglycemia/Diabetes Mellitus: Monitor glucose regularly in patients with and at risk for diabetes (5.6) o Dyslipidemia: Undesirable a …

Possible side effects

Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The following adverse reactions are discussed in more detail in other sections of the labeling: • Increased Mortality in Elderly Patients with Dementia-Related Psychosis [see Boxed Warning and Warnings and Precautions (5.1)] • Cerebrovascular Adverse Events, Including Stroke [see Warnings and Precautions (5.2)] • Suicidal Thoughts and Behaviors in Children, Adolescents, and Young Adults [see Boxed Warning and Warnings and Precaution …

Pregnancy and breastfeeding

8.1 Pregnancy Pregnancy Exposure Registry There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to atypical antipsychotics, including aripiprazole, during pregnancy. Healthcare providers are encouraged to register patients by contacting the National Pregnancy Registry for Atypical Antipsychotics at 1-866-961-2388 or visit http://womensmentalhealth.org/clinical-and-research-programs/pregnancyregistry/ . …

If you take too much

MedDRA terminology has been used to classify the adverse reactions. 10.1 Human Experience In clinical trials and in postmarketing experience, adverse reactions of deliberate or accidental overdosage with oral aripiprazole have been reported worldwide. These include overdoses with oral aripiprazole alone and in combination with other substances. No fatality was reported with aripiprazole alone. The largest known dose with a known outcome involved acute ingestion of 1,260 mg of oral aripiprazole (42 times the maximum recommended daily dose) by a patient who fully recovered. …

Dependence and misuse

9.1 Controlled Substance Aripiprazole is not a controlled substance. 9.2 Abuse Aripiprazole has not been systematically studied in humans for its potential for abuse, tolerance, or physical dependence. Consequently, patients should be evaluated carefully for a history of drug abuse, and such patients should be observed closely for signs of aripiprazole tablets misuse or abuse (e.g., development of tolerance, increases in dose, drug-seeking behavior). …

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 2026-03-05.

Label for aripiprazole, the active ingredient registered with NAFDAC.

Check your pack of Aqeud 10 Tablets

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

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3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About Aqeud 10 Tablets

What is in Aqeud 10 Tablets?

Aqeud 10 Tablets contains Aripiprazole (10 mg), as tablet, according to its NAFDAC registration record.

Is Aqeud 10 Tablets registered with NAFDAC?

Yes. Aqeud 10 Tablets is listed on the NAFDAC register under registration number B4-6029, and its registration is active as of 1 November 2026.

Has Aqeud 10 Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Aqeud 10 Tablets in our automatically synced alert list.

How can I check that my pack of Aqeud 10 Tablets is genuine?

Run a free authenticity scan with the NAFDAC number B4-6029, 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 Aqeud 10 Tablets?

Follow your prescription or the leaflet in your pack. The official label says: Initial Dose Recommended Dose Maximum Dose Schizophrenia – adults (2.1) 10 to 15 mg/day 10 to 15 mg/day 30 mg/day Schizophrenia – adolescents (2.1) 2 mg/day 10 mg/day 30 mg/day Irritability associated with autistic disorder – pediatric patients (2.4) 2 mg/day 5 to 10 mg/day 15 mg/day Tourette’s disorder – (2.5) Patients…

What is Aqeud 10 Tablets used for?

Aripiprazole is indicated for the treatment of: • Schizophrenia • Irritability Associated with Autistic Disorder • Treatment of Tourette’s Disorder Aripiprazole is an atypical antipsychotic. The oral formulations are indicated for: • Schizophrenia (14.1) • Irritability Associated with Autistic Disorder (14.4) • Treatment of Tourette’s disorder (14.5) (Summarised from the official U.S. FDA label for aripiprazole. Always follow your doctor or pharmacist.)

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