Consumer medicine information



Active ingredient(s): Methylprednisolone sodium succinate

Consumer Medicine Information (CMI)

This leaflet provides important information about using SOLU-MEDROL. You should also speak to your doctor or pharmacist if you would like further information or if you have any concerns or questions about using SOLU-MEDROL.

Where to find information in this leaflet:

1. Why am I given SOLU-MEDROL?
2. What should I know before I receive SOLU-MEDROL?
3. What if I am taking other medicines?
4. How is SOLU-MEDROL given?
5. What should I know while on SOLU-MEDROL?
6. Are there any side effects?
7. Product details

1. Why am I given SOLU-MEDROL?

SOLU-MEDROL contains the active ingredient methylprednisolone sodium succinate.

SOLU-MEDROL belongs to a group of medicine called corticosteroids. SOLU-MEDROL acts in the body by reducing inflammation (pain, swelling, redness and heat), which is one of the body’s reactions to injury, and by reducing the body’s reaction to infection.

SOLU-MEDROL is used to treat of one or more of the following:

  • skin diseases
  • allergic reactions
  • inflammation of the eyes
  • respiratory diseases and certain respiratory infections
  • diseases of the gut (gastrointestinal tract)
  • multiple sclerosis
  • rheumatic disorders
  • diseases of the blood
  • treatment of certain glandular conditions.

Your doctor may have prescribed SOLU-MEDROL for another reason.

There is no evidence that SOLU-MEDROL is addictive.

2. What should I know before I receive SOLU-MEDROL?


Do not use SOLU-MEDROL if:

  1. you are allergic to methylprednisolone sodium succinate or any of the ingredients listed at the end of this leaflet. The SOLU-MEDROL 40 mg product contains lactose from cow’s milk.
  2. Always check the ingredients to make sure you can use this medicine.
  3. you have a severe fungal infection.

Check with your doctor if you:

  • have or have had any of the following medical conditions:
    – disease of the heart, e.g., high blood pressure (hypertension) or congestive heart failure
    – condition or tumour of the adrenal and/or pituitary glands
    – stomach ulcers
    – thin or weak bones, or bones that tend to break easily (osteoporosis)
    – kidney or liver disease
    – underactive thyroid gland
    – emotional and mental disorder
    – myasthenia gravis (ongoing chronic fatigue and muscle weakness)
    – tuberculosis (TB)
    – herpes simplex of the eye
    – any pus producing infections
    – disease of the bowel, e.g., ulcerative colitis or diverticulitis
    – recent head injuries
    – fits or convulsions
    – diabetes or increased sugar in your blood
    – blood clots.
    If you are scheduled to have any laboratory tests, e.g., blood or urine, tell your doctor that you are being treated with SOLU-MEDROL.
    The use of SOLU-MEDROL may disguise the signs of infections due to a decrease in the body’s response to the infection. If you are in any doubt please consult your doctor.
  • take any medicines for any other condition
  • have recently been vaccinated or immunised. SOLU-MEDROL must not be used with certain types of vaccines
  • are allergic to any other medicines or any other substances such as foods, preservatives or dyes, especially cow’s milk or any other dairy products.

During treatment, you may be at risk of developing certain side effects. It is important you understand these risks and how to monitor for them. See additional information under Section 6. Are there any side effects?


Long term treatment with corticosteroids can affect growth and development in children. It can also increase the risk of high pressure in the brain. Your doctor will monitor your child closely if your child needs long term treatment with SOLU-MEDROL.

Some of the SOLU-MEDROL products contain benzyl alcohol. Benzyl alcohol has been associated with a rare but serious side effect in infants. Your doctor will decide if treatment is appropriate.


If you are over 65 years old, you may have an increased chance of side effects such as bone weakness possibly leading to fractures. You may also experience fluid retention which may lead to increased blood pressure.

If you have not told your doctor about any of the above, tell them before you start treatment with SOLU-MEDROL.

Pregnancy and breastfeeding

Check with your doctor if you are pregnant or intend to become pregnant.

Talk to your doctor if you are breastfeeding or intend to breastfeed.

Your doctor can discuss with you the risks and benefits involved.

3. What if I am taking other medicines?

Tell your doctor or pharmacist if you are taking any other medicines, including any medicines, vitamins or supplements that you buy without a prescription from your pharmacy, supermarket or health food shop.

Some medicines and food may interfere with SOLU-MEDROL and affect how it works. These include:

  • nonsteroidal anti-inflammatory such as salicylates or aspirin, medicines used to relieve pain, swelling and other symptoms of inflammation including arthritis.
  • neuromuscular blocking drugs, e.g., pancuronium
  • some antibiotics, e.g., erythromycin
  • medicines used to treat TB, e.g. isoniazid
  • some anti-fungal agents, e.g., ketoconazole, amphotericin
  • medicines to treat HIV, e.g., indinavir, ritonavir
  • some medicines to treat blood pressure, heart conditions and stroke, e.g., digoxin and diltiazem
  • some diuretics e.g., frusemide, a medicine to help kidneys get rid of salt and water by increasing the amount of urine produced
  • medicine for nausea, e.g., aprepitant, fosaprepitant
  • oral contraceptives
  • medicines used for myasthenia gravis, glaucoma, Alzheimer’s disease
  • medicines for psychiatric disorders
  • medicines to treat anxiety
  • bronchodilators (a type of medicine that opens up the airways in the lungs) used to treat asthma, bronchitis, emphysema, and other lung diseases, e.g., salbutamol
  • medicines to treat breast cancer or hormone disorder
  • anticonvulsants e.g., phenytoin, phenobarbitone
  • anticoagulants e.g., heparin, warfarin
  • antidiabetic medicines e.g., insulin, glibenclamide and metformin
  • immunosuppressants e.g., methotrexate and ciclosporin (a medicine used in kidney transplant patients)
  • some immunisations, inoculations or vaccinations
  • grapefruit juice.

Check with your doctor or pharmacist if you are not sure about what medicines, vitamins or supplements you are taking and if these affect SOLU-MEDROL.

4. How is SOLU-MEDROL given?

This medicine will be administered under medical supervision.

SOLU-MEDROL must be administered by intravenous or intramuscular injection. It must not be given in the spinal cord (intrathecal or epidural) or by local injection due to the risk of serious side effects.

You must not administer this medicine to yourself.

SOLU-MEDROL powder is reconstituted with the diluent provided or Sterile Water for Injections by your doctor or pharmacist.

How much you should be given

The dose and how often you are treated with SOLU-MEDROL will depend on your medical condition and also on your weight. Your doctor may change the dose and how many times a day you have it, as your condition changes.

Your doctor will continue giving you SOLU-MEDROL for as long as your condition requires.

If you are given too much SOLU-MEDROL

SOLU-MEDROL will be administered under medical supervision, so an overdose is unlikely.

However, repeated frequent doses over a long period of time may cause an increase in side effects.

If you think that you have been given too much SOLU-MEDROL, you may need urgent medical attention.

You should immediately:

  • contact your doctor, or
  • phone the Poisons Information Centre
    (by calling 13 11 26), or
  • go to the Emergency Department at your nearest hospital.

You should do this even if there are no signs of discomfort or poisoning.

Keep the telephone numbers for these services handy.

5. What should I know while on SOLU-MEDROL?

Things you should do

Tell your doctor immediately if you notice any unusual symptoms.

If you are about to start taking any new medicines, tell your doctor or pharmacist that you are being treated with SOLU-MEDROL.

Tell any doctor, dentist or pharmacist who treats you that you are being treated with SOLU-MEDROL.

Tell your doctor immediately if you become pregnant while taking SOLU-MEDROL.

If you are about to have any blood test, tell you doctor that you are taking SOLU-MEDROL.

It may interfere with some of the results.

Keep all your doctor’s appointments so that your progress can be checked.

Things you should not do

Avoid drinking grapefruit juice while you are being treated with SOLU-MEDROL.

Grapefruit may interact with SOLU-MEDROL and affect the way your body uses the medicine.

Driving or using machines

Be careful before you drive or use any machines or tools until you know how SOLU-MEDROL affects you.

SOLU-MEDROL may cause dizziness, light headedness, visual disturbances, and fatigue in some patients.

Do not drive or operate machinery or do anything else that could be dangerous, if you have any of these symptoms.

Looking after your medicine

Normally your doctor will get SOLU-MEDROL from the hospital pharmacy or their consulting rooms. If you do take your SOLU-MEDROL from the pharmacy to your doctor, it is important to store it in a safe place away from heat (below 25°C).

Do not leave SOLU-MEDROL in a car.

If for any reason you take your SOLU-MEDROL home, always ensure that it is stored in a place where children cannot reach it.

Getting rid of any unwanted medicine

If your doctor stops treating you with SOLU-MEDROL, your hospital pharmacist will dispose of any unused medicine.

The expiry date is printed on the labels. SOLU-MEDROL should not be used after this date has passed.

6. Are there any side effects?

Tell your doctor or pharmacist as soon as possible if you do not feel well while you are being treated with SOLU-MEDROL.

All medicines can have side effects. If you do experience any side effects, most of them are minor and temporary. However, some side effects may need medical attention.

See the information below and, if you need to, ask your doctor or pharmacist if you have any further questions about side effects.

Do not be alarmed by this list of possible side effects. You may not experience any of them.

Common side effects

Common side effects What to do
  • weight gain as a result of fluid retention or increased appetite
  • muscle weakness or loss of muscle mass
  • loss of ability to feel pain in the joint and instability of the joint
  • pain when putting weight or pressure on a joint
  • increased sweating
  • headache or dizziness
  • light headedness
  • changes in your menstrual periods
  • mood changes and other mental disorders such as memory loss, reduced perception and problem-solving abilities
  • nausea
  • vomiting
  • itchy or peeling skin
  • loss of appetite or weight loss
  • thin fragile skin or bruising
  • acne
  • facial redness or bands, stripes or lines on the skin
  • excessive hairiness, particularly in women
  • benign tumour-like lumps as a result of fat deposits in the tissues
  • persistent hiccups
  • stomach pain or discomfort
  • diarrhoea
  • fatigue or generally feeling unwell
  • pain, redness at the injection site.
Speak to your doctor if you have any of these common side effects and they worry you.

Serious side effects

Serious side effects What to do
Call your doctor immediately:

  • bone weakness possibly leading to fractures
  • wounds that will not heal
  • red, purple or brown patches on your skin
  • loss of sensation or problems with your reflexes (slow or too fast)
  • yellowing of the skin or eyes, dark urine, loss of appetite.

Seek Emergency medical attention:

  • signs of increased pressure in the skull, including drowsiness, vomiting, headache, weakness, numbness and /or eye problems such as double vision
  • convulsions or fits
  • blurred or loss of vision, distorted vision or a blind spot in your central vision, pressure in the eye
  • signs of frequent infections such as fever, severe chills, sore throat or mouth ulcers
  • allergic-type reactions, e.g., skin rash, itching and difficulty breathing, wheezing or coughing (anaphylactic reactions)
  • swelling of hands, ankles or feet
  • swelling of the face, lips, mouth, tongue or throat which may cause difficulty in swallowing or breathing
  • inflammation of the food pipe. You may experience difficulty or pain when swallowing or heartburn
  • poor appetite, fever, chills, nausea and a persistent stomach-ache that becomes worse with movement
  • uncomfortable or severe stomach pains or belching after eating
  • pain and tenderness in the leg, pain on extending the foot, swelling of the lower leg, ankle and foot
  • chest pain and breathlessness
Call your doctor straight away, or go straight to the Emergency Department at your nearest hospital if you notice any of these serious side effects.

Tell your doctor or pharmacist if you notice anything else that may be making you feel unwell.

SOLU-MEDROL can also cause chemical imbalances in the blood and urine, swelling of the pancreas (pancreatitis), bleeding in the stomach, masking of infections, increased risk of infection, hormone changes, metabolic changes, changes in liver enzymes, increased blood pressure or increased number of white blood cells (leucocytosis). Some of these side effects can only be found when your doctor does tests from time to time to check on your progress.

Other side effects not listed here may occur in some people.

Reporting side effects

After you have received medical advice for any side effects you experience, you can report side effects to the Therapeutic Goods Administration online at By reporting side effects, you can help provide more information on the safety of this medicine.

Always make sure you speak to your doctor or pharmacist before you decide to stop taking any of your medicines.

7. Product details

This medicine is only available with a doctor’s prescription.

What SOLU-MEDROL contains

Active ingredient
(main ingredient)
methylprednisolone sodium succinate
Other ingredients
(inactive ingredients)
40 mg ACT-O-VIAL System

  • monobasic sodium phosphate
  • dibasic sodium phosphate
  • lactose monohydrate
  • sodium hydroxide
  • water for injections (diluent)

125 mg ACT-O-VIAL System

  • monobasic sodium phosphate
  • dibasic sodium phosphate
  • sodium hydroxide
  • water for injections (diluent)

500 mg, 1 g and 2 g Vials with Diluent

  • monobasic sodium phosphate
  • dibasic sodium phosphate
  • sodium hydroxide
  • benzyl alcohol (diluent)
  • water for injections (diluent)

500 mg and 1 g Plain Vials

  • monobasic sodium phosphate
  • dibasic sodium phosphate
  • sodium hydroxide

Do not use this medicine if you are allergic to any of these ingredients.

What SOLU-MEDROL looks like

SOLU-MEDROL powder for injection is a white, or nearly white powder in a vial.

SOLU-MEDROL is supplied as:

  • one vial with separate sections containing the powder and the liquid to dissolve the powder ready for injection (ACT-O-VIAL system), or
  • two vials, one containing the powder and the other containing the liquid to dissolve the powder ready for injection, or
  • plain vials containing only the powder.

Available pack sizes:

40 mg ACT-O-VIAL – 5s pack (AUST R 171991)

125 mg ACT-O-VIAL – 1s pack (AUST R 171992)

500 mg vial with diluent – 1s pack (AUST R 12344)

1 g vial with diluent – 1s pack (AUST R 12340)

2 g vial with diluent – 1s pack (AUST R 12342)

500 mg plain vial – 1s and 5s pack (AUST R 50691)

1 g plain vial – 1s and 5s pack (AUST R 50698)

Not all presentations are available.

Who distributes SOLU-MEDROL

Pfizer Australia Pty Ltd
Sydney NSW
Toll Free Number: 1800 675 229

This leaflet was prepared in December 2021.