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Methylprednisolone Sodium Succinate for Injection

NAFDAC Reg. No. C4-1759 · Drug

Registered with NAFDAC. Registration activeAs of 2 November 2026 · synced automatically from official sources.
Product
Methylprednisolone Sodium Succinate for Injection
NAFDAC number
C4-1759
Active ingredient
Methylprednisolone sodium succinate
Strength
500 mg
Form
Powder for injection
Pack size
1 x 1's (in vials)
Manufacturer
Not listed
Applicant (holder)
Zadip Healthcare Ltd
Approved
3 Aug 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
2 Aug 2026
WHO alerts
None found
Community reports
None
Times checked
0

About the medicine: Methylprednisolone sodium succinate: uses, dosage and brands worldwide

What we found

  • Methylprednisolone Sodium Succinate for Injection is on the NAFDAC register with an active registration (C4-1759). 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 Methylprednisolone Sodium Succinate for Injection

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

Methylprednisolone tablets are indicated in the following conditions: 1. Endocrine Disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance). Congenital adrenal hyperplasia Nonsuppurative thyroiditis Hypercalcemia associated with cancer 2. …

How to take it and how often
  • The initial dosage of methylprednisolone tablets may vary from 4 mg to 48 mg of methylprednisolone per day depending on the specific disease entity being treated
  • In situations of less severity lower doses will generally suffice while in selected patients higher initial doses may be required
  • The initial dosage should be maintained or adjusted until a satisfactory response is noted
  • If after a reasonable period of time there is a lack of satisfactory clinical response, methylprednisolone tablets should be discontinued and the patient transferred to other appropriate therapy
  • IT SHOULD BE EMPHASIZED THAT DOSAGE REQUIREMENTS ARE VARIABLE AND MUST BE INDIVIDUALIZED ON THE BASIS OF THE DISEASE UNDER TREATMENT AND THE RESPONSE OF THE PATIENT
  • After a favorable response is noted, the proper maintenance dosage should be determined by decreasing the initial drug dosage in small decrements at appropriate time intervals until the lowest dosage which will maintain an adequate clinical response is reached
  • It should be kept in mind that constant monitoring is needed in regard to drug dosage
  • Included in the situations which may make dosage adjustments necessary are changes in clinical status secondary to remissions or exacerbations in the disease process, the patient's individual drug responsiveness, and the effect of patient exposure to stressful situations not directly related to the disease entity under treatment; in this latter situation it may be necessary to increase the dosage of methylprednisolone tablets for a period of time consistent with the patient's condition. …
While you are taking it
  • Information for the Patient Persons who are on immunosuppressant doses of corticosteroids should be warned to avoid exposure to chickenpox or measles
  • Patients should also be advised that if they are exposed, medical advice should be sought without delay
Talk to a doctor first if

Systemic fungal infections and known hypersensitivity to components.

Medicines it may not mix with

The pharmacokinetic interactions listed below are potentially clinically important. Mutual inhibition of metabolism occurs with concurrent use of cyclosporin and methylprednisolone; therefore, it is possible that adverse events associated with the individual use of either drug may be more apt to occur. Convulsions have been reported with concurrent use of methylprednisolone and cyclosporin. Drugs that induce hepatic enzymes such as phenobarbital, phenytoin and rifampin may increase the clearance of methylprednisolone and may require increases in methylprednisolone dose to achieve the desired response. …

Warnings

In patients on corticosteroid therapy subjected to unusual stress, increased dosage of rapidly acting corticosteroids before, during, and after the stressful situation is indicated. Corticosteroids may mask some signs of infection, and new infections may appear during their use. Infections with any pathogen including viral, bacterial, fungal, protozoan or helminthic infections, in any location of the body, may be associated with the use of corticosteroids alone or in combination with other immunosuppressive agents that affect cellular immunity, humoral immunity, or neutrophil function. 1 These infections may be mild, but can be severe and at times fatal. …

Possible side effects

Fluid and Electrolyte Disturbances Sodium retention Congestive heart failure in susceptible patients Hypertension Fluid retention Potassium loss Hypokalemic alkalosis Musculoskeletal Muscle weakness Loss of muscle mass Steroid myopathy Osteoporosis Tendon rupture, particularly of the Achilles tendon Vertebral compression fractures Aseptic necrosis of femoral and humeral heads Pathologic fracture of long bones Gastrointestinal Peptic ulcer with possible perforation and hemorrhage Pancreatitis Abdominal distention Ulcerative esophagitis Increases in alanine transaminase (ALT, SGPT), aspartate transaminase (AST, SGOT), and alkaline phosphatase have been observed following corticosteroid treatme …

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 2024-04-12.

Label for methylprednisolone sodium succinate, the active ingredient registered with NAFDAC.

Check your pack of Methylprednisolone Sodium Succinate for Injection

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 Methylprednisolone Sodium Succinate for Injection

What is in Methylprednisolone Sodium Succinate for Injection?

Methylprednisolone Sodium Succinate for Injection contains Methylprednisolone sodium succinate (500 mg), as powder for injection, according to its NAFDAC registration record.

Is Methylprednisolone Sodium Succinate for Injection registered with NAFDAC?

Yes. Methylprednisolone Sodium Succinate for Injection is listed on the NAFDAC register under registration number C4-1759, and its registration is active as of 2 November 2026.

Has Methylprednisolone Sodium Succinate for Injection been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Methylprednisolone Sodium Succinate for Injection in our automatically synced alert list.

How can I check that my pack of Methylprednisolone Sodium Succinate for Injection is genuine?

Run a free authenticity scan with the NAFDAC number C4-1759, 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 Methylprednisolone Sodium Succinate for Injection?

Follow your prescription or the leaflet in your pack. The official label says: The initial dosage of methylprednisolone tablets may vary from 4 mg to 48 mg of methylprednisolone per day depending on the specific disease entity being treated. In situations of less severity lower doses will generally suffice while in selected patients higher initial doses may be required. The initial dosage should be maintained or adjusted until a satisfactory response is n…

What is Methylprednisolone Sodium Succinate for Injection used for?

Methylprednisolone tablets are indicated in the following conditions: 1. Endocrine Disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance). Congenital adrenal hyperplasia Nonsuppurative (Summarised from the official U.S. FDA label for methylprednisolone sodium succinate. Always follow your doctor or pharmacist.)

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