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Methylprednisolone

Methylprednisolone tablets are indicated in the following conditions: 1. Endocrine Disorders Primary or secondary adrenocortical insufficiency (hydroc.

Prescription medicine 口服 Safety alerts on record

How to use Methylprednisolone

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.

Brands around the world

Products with Methylprednisolone as the active ingredient. Names differ between countries.

Registered products

United States (FDA)

MethylprednisoloneMETHYLPREDNISOLONE 32 mg/1 · Tablet · Chartwell RX, LLC
NDC 62135-763Label
Depo-medrolMETHYLPREDNISOLONE ACETATE 40 mg/mL · Injection, Suspension · A-S Medication Solutions
NDC 50090-2098Label
MethylprednisoloneMETHYLPREDNISOLONE 8 mg/1 · Tablet · Chartwell RX, LLC
NDC 62135-761Label
MethylprednisoloneMETHYLPREDNISOLONE 16 mg/1 · Tablet · Chartwell RX, LLC
NDC 62135-762Label
Methylprednisolone Sodium SuccinateMETHYLPREDNISOLONE SODIUM SUCCINATE 40 mg/mL · Injection, Powder, Lyophilized, For Solution · Fresenius Kabi USA, LLC
NDC 63323-255Label

Nigeria (NAFDAC)

NAFDACMethylprednisolone Sodium Succinate for Injection C4-1759NAFDACNeofidrol Lotion A11-100071NAFDACNeofidrol Lotion A11-1128NAFDACNeo-Medrol Lotion 04-3778NAFDACNeo Presol Lotion_ 04-2017

Other countries: check your pack's registration number and we point you to your regulator.

Safety alerts and recalls

methylprednisolone tablets, USP Dosepak, 4 mg, 1 Blister Card per Carton containing 21 Tablets, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977. NDC 59762-4440-2U.S. FDA Class II
15 Jan 2026 · Greenstone Llc · OngoingLabeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing information when following the directions on the foil.
MethylPREDNISolone Acetate Injectable Suspension, USP, 400 mg per 10 mL (40 mg per mL), 1 x 10 mL Multi-Dose Vial, Rx only, Mfd. for SAGENT Pharmaceuticals, Schaumburg, IL 60195, U.S. FDA Class II
25 Apr 2024 · Sagent Pharmaceuticals · OngoingPresence of Particulate Matter: Potential for black particulates in the drug product.
Methylprednisolone acetate Injectable Suspension, USP, 400mg per 5mL (80mg/mL, 5mL Multiple-Dose Vial, Rx only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ 08520, NDC 55150-314U.S. FDA Class II
20 Feb 2024 · Eugia US LLC · OngoingFailed Dissolution Specifications
Methylprednisolone Acetate Injectable Suspension, USP 80 mg/mL, For Intramuscular, Intrasynovial and Soft Tissue Injection Only, Not for Intravenous Use, 1 mL Single Dose Vial, ManU.S. FDA Class III
8 May 2023 · Amneal Pharmaceuticals of New York, LLC · TerminatedLabeling: Not Elsewhere Classified; A typographical error was observed in the NDC number on the preprinted Individual Folding Cartons (secondary packaging only). Incorrect NDC Number 70121-1573-1; Correct NDC Number 70121-1574-1.

A recall usually affects certain batches only. Compare the lot number on your pack.

Check your pack of Methylprednisolone

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

Questions about Methylprednisolone

What is Methylprednisolone 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 thyroiditis Hyperca (From the official U.S. FDA label.)

How do I take Methylprednisolone?

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…

Do I need a prescription for Methylprednisolone?

Usually yes. Methylprednisolone is a prescription medicine in most countries. Rules differ by country.

What brands contain Methylprednisolone?

Methylprednisolone is sold under names such as Hybrisil, Medrol, Solu-medrol, Depo-medrol, Methylprednisolone. Brand names differ between countries.

How can I check that my Methylprednisolone is genuine?

Scan the registration number on your pack with PillVera (NAFDAC number in Nigeria, NDC in the United States, DIN in Canada), check the expiry date and buy only from licensed pharmacies.