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Drug: methylprednisolone sodium succinate
Brand: Solu-Medrol 125mg
Manufacturer /
TM Owner
Pfizer
Origin: USA

Solu-Medrol 125mg Injection

Solu-Medrol contains methylprednisolone sodium succinate, a corticosteroid. It suppresses inflammation and immune overactivity, relieving swelling, itching and allergic or autoimmune symptoms. It is used in the treatment of critical and intensive care. It is supplied as an injection (125mg). Available on prescription, it forms part of modern, guideline-driven care.
Strength: 125mg
Pack Size: 1s
Storage: 20°C to 25°C
Form: Injection

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Indications & Clinical Uses

  • Solu-Medrol 125mg is the injectable form of methylprednisolone sodium succinate, a potent synthetic glucocorticoid marketed by Pfizer (labeled by its Pharmacia & Upjohn division).
  • Given as an intravenous or intramuscular injection by a healthcare provider when oral steroid therapy is not feasible or a rapid effect is needed, it is approved for severe allergic reactions and status asthmaticus, dermatologic diseases such as pemphigus and Stevens-Johnson syndrome, hematologic disorders such as autoimmune haemolytic anaemia, acute exacerbations of multiple sclerosis, cerebral oedema associated with brain tumours or surgery, rheumatic disorders including systemic lupus erythematosus and rheumatoid arthritis, respiratory conditions such as sarcoidosis, gastrointestinal, renal and ophthalmic inflammatory disease, and certain cancers as adjunctive therapy.
  • High-dose, short pulse regimens are used for acute MS relapse under specialist supervision.
  • Solu-Medrol is given only by or under the supervision of a healthcare professional in a hospital or clinic setting, not for home self-injection.

Side Effects

  • Common reactions after methylprednisolone sodium succinate injection include fluid retention, raised blood pressure, mood or sleep disturbance, increased appetite, flushing, and a metallic taste or brief perineal burning if the injection is given too quickly.
  • With high-dose or repeated use, more serious effects can occur, including hyperglycaemia, Cushingoid features, osteoporosis and fractures, myopathy, psychiatric disturbances including psychosis, peptic ulcer with possible perforation, pancreatitis, and increased susceptibility to infection with suppressed signs of infection.
  • Rare but serious cardiac events, including arrhythmias, bradycardia, cardiac arrest and, very rarely, myocardial rupture after recent heart attack, have been reported, mainly with rapid high-dose administration.
  • As with other injectable corticosteroids, the label carries a prominent warning that serious, sometimes fatal, neurologic events, including stroke and paraplegia, have followed epidural corticosteroid injection; Solu-Medrol is not approved for and must never be given by the epidural or intrathecal route.
  • Seek urgent help for chest pain, severe abdominal pain, black stools, sudden weakness, or signs of infection.

Precautions & Warnings

  • Solu-Medrol is contraindicated in patients with systemic fungal infections and known hypersensitivity to methylprednisolone or any component; intrathecal and epidural administration are not approved and must never be used because of the risk of serious neurologic events, and intramuscular use is contraindicated in idiopathic thrombocytopenic purpura.
  • Formulations preserved with benzyl alcohol must not be used in neonates or premature infants because of the risk of a fatal 'gasping syndrome'; the 40mg strength is also contraindicated in patients with known hypersensitivity to cow's milk protein.
  • Rapid intravenous administration of high doses has been associated with cardiovascular collapse, so high-dose infusions are given slowly over at least 30 minutes.
  • Use with caution in diabetes, hypertension, heart failure, recent myocardial infarction, peptic ulcer disease, osteoporosis, glaucoma, seizure disorders, myasthenia gravis and active or latent infections including tuberculosis.
  • Live vaccines should be avoided during high-dose therapy.
  • Use in pregnancy or breastfeeding only if benefit outweighs risk, and taper the dose gradually rather than stopping abruptly after prolonged treatment.

Avoid Interactions

  • Tell your healthcare provider about all medicines and supplements you use.
  • Drugs that increase methylprednisolone's effect or toxicity include CYP3A4 inhibitors such as ketoconazole, itraconazole, clarithromycin and ritonavir; combining Solu-Medrol with NSAIDs or aspirin raises the risk of gastrointestinal ulceration and bleeding; and use with potassium-depleting diuretics or amphotericin B can cause severe hypokalaemia, which can be dangerous with digoxin.
  • Anticholinesterase drugs used for myasthenia gravis combined with corticosteroids can cause severe generalised weakness.
  • Corticosteroids can reduce or unpredictably alter warfarin's effect, needing closer clotting monitoring, and can blunt the response to vaccines, so live vaccines should be avoided during high-dose therapy.
  • CYP3A4 inducers such as rifampin, phenytoin, carbamazepine and phenobarbital can reduce methylprednisolone's effect.
  • In diabetes, corticosteroids raise blood glucose and may need adjustment of antidiabetic medicines.
  • Solu-Medrol should not be mixed with other medicines in the same syringe or infusion unless compatibility is confirmed.

References

Frequently Asked Questions

Solu-Medrol (methylprednisolone sodium succinate) is an injectable corticosteroid used for severe allergic reactions, asthma flares, autoimmune and skin diseases, acute multiple sclerosis relapses, and swelling around brain tumours or after surgery, when oral steroids are not suitable.

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