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Nyumbani / Registered in Nigeria / Multichris Atenolol BP 100 mg Tablets

Multichris Atenolol BP 100 mg Tablets

NAFDAC Reg. No. B4-7530 · Drug

Registered with NAFDAC. Registration activeAs of 2 November 2026 · synced automatically from official sources.
Product
Multichris Atenolol BP 100 mg Tablets
NAFDAC number
B4-7530
Active ingredient
Atenolol
Strength
100 mg
Form
Tablet
Pack size
2 x 14's (in blisters)
Manufacturer
Not listed
Applicant (holder)
Multichris Pharmaceutical and Chemical Company Limited
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: Atenolol: uses, dosage and brands worldwide

What we found

  • Multichris Atenolol BP 100 mg Tablets is on the NAFDAC register with an active registration (B4-7530). 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 Multichris Atenolol BP 100 mg Tablets

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

Who it is for

Hypertension Atenolol tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including atenolol. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than 1 drug to achieve blood pressure goals. …

How to take it and how often
  • Hypertension The initial dose of atenolol is 50 mg given as one tablet a day either alone or added to diuretic therapy
  • The full effect of this dose will usually be seen within one to two weeks
  • If an optimal response is not achieved, the dosage should be increased to atenolol 100 mg given as one tablet a day
  • Increasing the dosage beyond 100 mg a day is unlikely to produce any further benefit
  • Atenolol may be used alone or concomitantly with other antihypertensive agents including thiazide-type diuretics, hydralazine, prazosin, and alpha-methyldopa
  • Angina Pectoris The initial dose of atenolol is 50 mg given as one tablet a day
  • If an optimal response is not achieved within one week, the dosage should be increased to atenolol 100 mg given as one tablet a day
  • Some patients may require a dosage of 200 mg once a day for optimal effect
  • Twenty-four hour control with once daily dosing is achieved by giving doses larger than necessary to achieve an immediate maximum effect
  • The maximum early effect on exercise tolerance occurs with doses of 50 mg to 100 mg, but at these doses the effect at 24 hours is attenuated, averaging about 50% to 75% of that observed with once a day oral doses of 200 mg
  • Acute Myocardial Infarction In patients with definite or suspected acute myocardial infarction, treatment with atenolol I.V. injection should be initiated as soon as possible after the patient's arrival in the hospital and after eligibility is established. …
Children
  • Safety and effectiveness
  • In pediatric patients have not been established
Older adults

Hypertension and Angina Pectoris Due to Coronary Atherosclerosis Clinical studies of atenolol did not include sufficient number of patients aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. …

While you are taking it
  • Hypoglycemia Inform patients or caregivers that there is a risk of hypoglycemia when atenolol is given to patients who are fasting or who are vomiting
  • Monitor for symptoms of hypoglycemia
Talk to a doctor first if

Atenolol tablets are contraindicated in sinus bradycardia, heart block greater than first degree, cardiogenic shock, and overt cardiac failure. (See WARNINGS .) Atenolol tablets are contraindicated in those patients with a history of hypersensitivity to the atenolol or any of the drug product’s components.

Medicines it may not mix with

Catecholamine-depleting drugs (e.g., reserpine) may have an additive effect when given with beta-blocking agents. Patients treated with atenolol plus a catecholamine depletor should therefore be closely observed for evidence of hypotension and/or marked bradycardia which may produce vertigo, syncope, or postural hypotension. Calcium channel blockers may also have an additive effect when given with atenolol (see WARNINGS ). Disopyramide is a Type I antiarrhythmic drug with potent negative inotropic and chronotropic effects. Disopyramide has been associated with severe bradycardia, asystole and heart failure when administered with beta-blockers. …

Warnings

Cardiac Failure Sympathetic stimulation is necessary in supporting circulatory function in congestive heart failure, and beta-blockade carries the potential hazard of further depressing myocardial contractility and precipitating more severe failure. In patients with acute myocardial infarction, cardiac failure which is not promptly and effectively controlled by 80 mg of intravenous furosemide or equivalent therapy is a contraindication to beta-blocker treatment. In Patients Without a History of Cardiac Failure Continued depression of the myocardium with beta-blocking agents over a period of time can, in some cases, lead to cardiac failure. …

Possible side effects

Most adverse effects have been mild and transient. The frequency estimates in the following table were derived from controlled studies in hypertensive patients in which adverse reactions were either volunteered by the patient (U.S. studies) or elicited, e.g., by checklist (foreign studies). The reported frequency of elicited adverse effects was higher for both atenolol and placebo-treated patients than when these reactions were volunteered. Where frequency of adverse effects of atenolol and placebo is similar, causal relationship to atenolol is uncertain. Volunteered (U.S. Studies) Total - Volunteered and Elicited (Foreign + U.S. …

Pregnancy and breastfeeding

Pregnancy See WARNINGS - Pregnancy and Fetal Injury .

If you take too much

Overdosage with atenolol has been reported with patients surviving acute doses as high as 5 g. One death was reported in a man who may have taken as much as 10 g acutely. The predominant symptoms reported following atenolol overdose are lethargy, disorder of respiratory drive, wheezing, sinus pause and bradycardia. Additionally, common effects associated with overdosage of any beta-adrenergic blocking agent and which might also be expected in atenolol overdose are congestive heart failure, hypotension, bronchospasm and/or hypoglycemia. …

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 2024-11-26.

Label for atenolol, the active ingredient registered with NAFDAC.

Check your pack of Multichris Atenolol BP 100 mg Tablets

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

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About Multichris Atenolol BP 100 mg Tablets

What is in Multichris Atenolol BP 100 mg Tablets?

Multichris Atenolol BP 100 mg Tablets contains Atenolol (100 mg), as tablet, according to its NAFDAC registration record.

Is Multichris Atenolol BP 100 mg Tablets registered with NAFDAC?

Yes. Multichris Atenolol BP 100 mg Tablets is listed on the NAFDAC register under registration number B4-7530, and its registration is active as of 2 November 2026.

Has Multichris Atenolol BP 100 mg Tablets been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Multichris Atenolol BP 100 mg Tablets in our automatically synced alert list.

How can I check that my pack of Multichris Atenolol BP 100 mg Tablets is genuine?

Run a free authenticity scan with the NAFDAC number B4-7530, 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 Multichris Atenolol BP 100 mg Tablets?

Follow your prescription or the leaflet in your pack. The official label says: Hypertension The initial dose of atenolol is 50 mg given as one tablet a day either alone or added to diuretic therapy. The full effect of this dose will usually be seen within one to two weeks. If an optimal response is not achieved, the dosage should be increased to atenolol 100 mg given as one tablet a day. Increasing the dosage beyond 100 mg a day is unlikely to produce any…

What is Multichris Atenolol BP 100 mg Tablets used for?

Hypertension Atenolol tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including atenolol. Control of high blood (Summarised from the official U.S. FDA label for atenolol. Always follow your doctor or pharmacist.)

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