Consumer Medicine Information
What is in this leaflet
Please read this leaflet carefully before being treated with DEPO-MEDROL suspension
for injection. This leaflet answers some common questions about DEPO-MEDROL. It
does not contain all the available information. It does not take the place of talking
to your doctor or pharmacist.
All medicines have risks and benefits. Your doctor has weighed the risks of you being
treated with DEPO-MEDROL against the benefits this medicine is expected to have for
If you have any concerns about this medicine, ask your doctor or pharmacist.
Consider keeping this leaflet even after treatment with DEPO-MEDROL is finished.
You may need to read it again.
What DEPO-MEDROL is used for
DEPO-MEDROL is used to treat disorders of many organ systems such as skin, lung, eye,
gastrointestinal tract, nervous system, joints and blood. DEPO-MEDROL works by reducing
inflammation and changing the body's natural ability to respond when the immune response
is not working properly. It is also used in certain conditions where the adrenal
gland doesn't function correctly.
Your doctor may have prescribed DEPO-MEDROL for another reason.
Ask your doctor if you have any questions about why DEPO-MEDROL has been prescribed
This medicine is available only with a doctor's prescription.
Before treatment with DEPO-MEDROL
Some information is provided below. However, always talk to your doctor if you have
concerns or questions about your treatment.
When DEPO-MEDROL must not be used
DEPO-MEDROL must not be used:
1. if you have an allergy to:
any of the other ingredients listed under Product Description at the end of this leaflet.
Symptoms of an allergic reaction may include skin rash, itching or difficulty in breathing.
2. if you have a severe fungal infection
3. it must not be injected into the spinal cord (intrathecal or epidural) or into a vein
4. it must not be given by any other unapproved route of administration
5. if you have been given a vaccine
6. if the packaging is torn or shows signs of tampering
7. after the expiry date (EXP) printed on the carton.
If you use it after the expiry date, it may have no effect at all, or an entirely
If you are not sure whether you should be treated with DEPO-MEDROL, talk to your doctor.
Before treatment with DEPO-MEDROL
Before treatment with DEPO-MEDROL, tell your doctor if:
1. you are pregnant or intend to become pregnant
Your doctor will discuss the risks and benefits of using DEPO-MEDROL during pregnancy.
2. you are breastfeeding or plan to breastfeed
Your doctor will discuss the risks and benefits of using DEPO-MEDROL when breastfeeding.
3. you have allergies to any other medicines or any other substances such as foods, preservatives
4. you have or have had any of the following:
underactive thyroid gland
kidney or liver disease
herpes in the eye
hypoprothrombinaemia (a blood clotting disorder)
disease of the bowel, e.g., ulcerative colitis or diverticulitis
emotional problems or mental disorder
any pus-producing infection
problems with your heart, including high blood pressure or congestive heart failure
Cushing's disease (a hormone disorder)
seizure disorders e.g. epilepsy
myasthenia gravis (ongoing muscle weakness and chronic fatigue)
thin or weak bones, or bones that tend to break easily (osteoporosis)
recent head injuries
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 DEPO-MEDROL.
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, do so before you are treated
Taking other medicines
Tell your doctor if you are taking any other medicines, including medicines that you
buy without a prescription from a pharmacy, supermarket or health food shop.
Some medicines or food and DEPO-MEDROL may interfere with each other. Some of these
medicines and food include:
cyclosporin, cyclophosphamide, tacrolimus (medicines used to suppress the immune system
e.g. after a transplant)
isoniazid (a medicine to treat tuberculosis)
non-steroidal anti-inflammatory drugs [NSAID] such as salicylates or aspirin (medicines
used to relieve pain, swelling and other symptoms of inflammation including arthritis)
some antifungals e.g. ketoconazole, itraconazole
some antibiotics e.g. rifampicin, erythromycin, clarithromycin
phenobarbitone, phenytoin, carbamazepine (medicines used to treat epilepsy, convulsions)
anticoagulants e.g. warfarin, heparin
some immunisations, inoculations or vaccinations
some diuretics e.g. frusemide, a medicine to help kidneys get rid of salt and water
by increasing the amount of urine produced
neuromuscular blocking drugs (medicines that block nerve and muscle action) e.g. pancuronium
medicines used to treat myasthenia gravis (ongoing muscle weakness and chronic fatigue),
glaucoma, Alzheimer's disease
medicines used to treat psychiatric disorders
medicines used 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 used to treat diabetes e.g. insulin, glibenclamide and metformin
anti-nausea medicines e.g. aprepitant, fosaprepitant
medicines to treat HIV e.g. indinavir, ritonavir
some medicines to treat blood pressure, heart conditions and stroke, e.g., digoxin
oral contraceptives e.g. ethinylestradiol, norethisterone
medicines used to treat breast cancer and hormone disorders.
These medicines and food may be affected by DEPO-MEDROL or may affect how well it
works. You may need different amounts of your medicine or you may need to take different
Your doctor or pharmacist can tell you what to do if you are taking any of these medicines.
They also have a more complete list of medicines to be careful with or avoid while
being treated with DEPO-MEDROL.
Ask your doctor or pharmacist if you are not sure if you are taking any of these medicines.
Treatment with DEPO-MEDROL
This medicine will be administered under medical supervision.
It may be given into a muscle (intramuscularly) or into a joint (intra-articularly)
or into a lesion (intralesional). Due to the risk of serious side effects, it must
not be injected into the spinal cord (intrathecally or epidural) or into a vein (intravenously).
How and where DEPO-MEDROL is injected and the dose given will depend on the nature
and the severity of your condition. You will be given a different dosage depending
on your condition and how you react to the medicine.
If you are given too much (overdose)
Overdose is unlikely with DEPO-MEDROL. However, repeated frequent doses over a long
period of time may cause an increase in side effects.
Immediately telephone your doctor or Poisons Information Centre (telephone 13 11 26)
for advice, or go to Accident and Emergency (Casualty) at your nearest hospital if
you think that you or anyone else may have been given too much DEPO-MEDROL. Do this
even if there are no signs of discomfort or poisoning. You may need urgent medical
attention. Keep the telephone numbers for these services handy. Have the DEPO-MEDROL
box or this leaflet available to give details if needed.
While you are being treated with it
Things you must do
If you become pregnant while you are being treated with DEPO-MEDROL, tell your doctor.
If you are about to start taking any new medicines, tell your doctor and pharmacist
that you are being treated with DEPO-MEDROL.
Tell all doctors, dentists and pharmacists who are treating you that you are being
treated with DEPO-MEDROL.
Tell your doctor that you are being treated with DEPO-MEDROL:
before having any skin tests
before having any kind of surgery
if you get a serious injury or infection.
Medicines such as DEPO-MEDROL can increase the risk of infection and mask symptoms
Tell your doctor if you notice any of the following:
sore or swollen joints.
Your doctor may request you follow a low-salt diet and/or take potassium supplements.
If you are a diabetic, your need for insulin or glucose lowering medicines may increase
while being treated with DEPO-MEDROL.
For patients having this medicine injected into their joints:
be careful not to put too much stress onto that joint for a while
ask your doctor how much you can move this joint while it is healing.
Your doctor may reduce the dose of DEPO-MEDROL gradually if you have been on long-term
Check with your doctor as soon as possible if you have any concerns while being treated
with DEPO-MEDROL, even if you do not think the concerns are connected with the medicine
or are not listed in this leaflet.
Like other medicines, DEPO-MEDROL can cause side effects. If they occur, most are
likely to be minor and temporary. However, some may be serious and need medical attention.
Ask your doctor or pharmacist to answer any questions you may have.
Tell your doctor if you notice any of the following and it worries you:
headache or dizziness
mood changes e.g. over-excitement, depression, suicidal thoughts, hallucinations,
changes to menstrual periods
muscle weakness, pain or loss of muscle mass
problems with your joints, including pain
problems with your growth
thin fragile skin or bruising
itchy or peeling skin
changes to skin at the injection site
rashes, acne, hives
diarrhoea or constipation
loss of appetite or weight loss
Tell your doctor immediately if you experience any of the following
bone weakness (can lead to fractures)
wounds that will not heal
loss in the control of your diabetes
red, purple or brown patches on your skin
problems with your back, including pain or weakness
loss of sensation or problems with your reflexes (slow or too fast)
bouts of anxiety and headaches, sweating, palpitations, dizziness, a feeling of weakness,
nausea, vomiting, diarrhoea, dilated pupils and blurring vision, stomach pains, and
raised blood pressure. These could be symptoms of a rare tumour of the adrenal gland,
which sits near the kidney.
Tell your doctor immediately, or go to Accident and Emergency at your nearest hospital
if you notice any of the following symptoms:
signs of increased pressure in the skull, including drowsiness, vomiting, headache,
weakness, numbness and /or eye problems such as double vision
allergic type reactions e.g. skin rash, itching and difficulty breathing, wheezing
or coughing, chest pain (anaphylactic reaction)
signs of infection such as fever, severe chills, sore throat or mouth ulcers
severe stomach pains
blurred or distorted vision or loss of vision, eye infections
breathlessness, fatigue and swelling (heart failure)
convulsions or fits
passing large amounts of urine, increased thirst and appetite
pain and tenderness in the leg, pain on extending the foot, swelling of the lower
leg, ankle and foot
chest pain and breathlessness.
DEPO-MEDROL can also cause chemical imbalances in the blood, swelling of the pancreas
(pancreatitis), masking of infections, increased risk of infection, hormone changes,
metabolic changes and changes in liver enzymes, increased blood pressure, increased
number of white blood cells (leucocytosis), or cataracts. Some of these side effects
can only be found when your doctor does tests to check on your progress.
This is not a complete list of all possible side effects. Some people may get other
side effects while being treated with DEPO-MEDROL.
It is very important to tell your doctor if you notice any side effects while being
treated with DEPO-MEDROL.
Do not be alarmed by this list of possible side effects.
You may not experience any of them.
After treatment with DEPO-MEDROL
DEPO-MEDROL will normally be stored in a hospital or doctor's surgery. It should
be stored in its original packaging in a cool, dry place where the temperature stays
below 30°C. It must not be frozen.
What it looks like
DEPO-MEDROL is a suspension for injection packaged in a glass vial. It is supplied
in cartons of 5 x 1 mL or 1 x 1 mL vials.
The active ingredient in DEPO-MEDROL is methylprednisolone acetate. Each vial contains
40 mg of methylprednisolone acetate.
DEPO-MEDROL also contains macrogol 3350, sodium chloride and miripirium chloride.
DEPO-MEDROL can be identified by the Australian Register Number, AUST R 12299, which
is found on the carton label.
DEPO-MEDROL is supplied in Australia by:
Pfizer Australia Pty Ltd
ABN 50 008 422 348
38-42 Wharf Road
West Ryde NSW 2114
Toll free number: 1800 675 229
This leaflet was revised in May 2018.
© Pfizer Australia Pty Ltd 2013