REPAGLINIDE MYLAN 1 MG TABLETS
Active substance(s): REPAGLINIDE
Read all of this leaflet carefully before you
start taking this medicine because it contains
important information for you.
• Keep this leaflet. You may need to read it again.
• If you have any further questions, ask your doctor
• This medicine has been prescribed for you. Do
not pass it on to others. It may harm them, even if
their signs of illness are the same as yours.
• If you get any side effects talk to your doctor
or pharmacist. This includes any possible side
effects not listed in this leaflet. See section 4.
What is in this leaflet:
1. What Repaglinide is and what it is used for
2. What you need to know before you take Repaglinide
3. How to take Repaglinide
4. Possible side effects
5. How to store Repaglinide
6. Contents of the pack and other information
1. WHAT REPAGLINIDE IS AND WHAT IT IS
Repaglinide is an oral antidiabetic agent containing
repaglinide which helps your pancreas produce more
insulin and thereby lower your blood sugar (glucose).
Type 2 diabetes is a disease in which your pancreas
does not make enough insulin to control the sugar
in your blood or where your body does not respond
normally to the insulin it produces (formerly known
as non-insulin-dependent diabetes mellitus or maturity
Repaglinide is used to control type 2 diabetes as
an add-on to diet and exercise: treatment is usually
started if diet, exercise and weight reduction alone
have not been able to control (or lower) your blood
sugar. Repaglinide can also be given with metformin,
another medicine for diabetes.
2. WHAT YOU NEED TO KNOW BEFORE YOU
Do not take Repaglinide if you
• are allergic (hypersensitive) to repaglinide or any
of the other ingredients of this medicine (listed in
• suffer from type 1 (insulin dependent) diabetes
• have been diagnosed with raised body acid levels (a
condition called diabetic ketoacidosis)
• suffer from severe liver disease
• take gemfibrozil (a medicine used to lower
increased fat levels in the blood)
If any of these apply to you, tell your doctor and do
not take Repaglinide.
Warnings and precautions
Talk to your doctor or pharmacist before
Take special care:
• if you suffer from liver problems. Repaglinide is not
recommended if you have moderate liver disease
and should not be taken if you have severe liver
disease (see 'Do not take Repaglinide').
• if you have kidney problems. Repaglinide should
be taken with caution.
• if you have recently had major surgery or suffered
from a severe illness or infection because your
body's glycaemic control may have been affected.
In these cases your doctor may advise you to stop
taking repaglinide and prescribe insulin until your
blood sugar levels have stabilised.
• if you are under 18 or over 75 years of age.
Repaglinide is not recommended. It has not been
studied in these age groups.
If any of the above applies to you, Repaglinide may
not be suitable for you. Your doctor will advise you.
If you get a hypo
You may get a hypo (short for a hypoglycaemic
reaction and is a symptom of low blood sugar) if your
blood sugar gets too low. This may happen:
• if you take too much Repaglinide
• if you exercise more than usual
• if you take other medicines or suffer from liver or
kidney problems (see other sections of 2. 'What you
need to know before you take Repaglinide').
The warning signs of a hypo may come on
suddenly and can include: cold sweat; cool pale skin;
headache; rapid heartbeat; feeling sick; feeling very
hungry; temporary changes in vision; drowsiness;
unusual tiredness and weakness; nervousness or
tremor; feeling anxious; feeling confused; difficulty in
If your blood sugar is low or you feel a hypo coming
on: eat glucose tablets or a high sugar snack or drink,
When the symptoms of hypoglycaemia have
disappeared or when your blood sugar levels are
stabilised continue with your Repaglinide treatment.
Tell people you have diabetes and that if you pass
out (become unconscious) due to a hypo, they must
turn you on your side and get medical help straight
away. They must not give you any food or drink. It
could choke you.
• If severe hypoglycaemia is not treated, it can cause
brain damage (temporary or permanent) and
• If you have a hypo that makes you pass out, or a
lot of hypos, talk to your doctor. The amount of
Repaglinide, food or exercise may need to
If your blood sugar gets too high
Your blood sugar may get too high (hyperglycaemia).
This may happen:
• if you take too little Repaglinide
• if you have an infection or a fever
• if you eat more than usual
• if you exercise less than usual.
The warning signs appear gradually. They include:
increased urination; feeling thirsty; dry skin and
dry mouth. Talk to your doctor. The amount of
Repaglinide, food or exercise may need to
Other medicines and Repaglinide
Tell your doctor or pharmacist if you are taking or
have recently taken any other medicines.
You can take Repaglinide with metformin (another
medicine for diabetes) if your doctor prescribes it.
If you are already taking another medicine for your
diabetes and you are also prescribed repaglinide,
please tell your doctor before you start to take
Do not take repaglinide if you are already taking
gemfibrozil to lower fat levels in your blood.
Your body's response to repaglinide may change if
you are also taking any of the following medicines:
• monoamine oxidase inhibitors (MAOI) used to
• beta-blockers used to treat high blood pressure or
• ACE-inhibitors used to treat heart conditions
• salicylates (such as aspirin)
• non-steroidal anti-inflammatory drugs (NSAIDs)
used as painkillers
• octreotide used to treat some cancers
• steroids (both anabolic steroids and corticosteroids)
used to treat anaemia or inflammation
• oral contraceptives (birth control pills)
• thiazides (referred to as diuretics or 'water pills')
• danazol to treat breast cysts and endometriosis
• thyroid products (used to treat low levels of
• sympathomimetics used to treat asthma
• clarithromycin, trimethoprim or rifampicin to treat
bacterial infections (antibiotic medicines)
• gemfibrozil (used to treat high blood fats)
• ciclosporin (used to suppress the immune system)
• deferasirox (used to reduce chronic iron overload)
• itraconazole or ketoconazole to treat fungal infections
• phenytoin, carbamazepine or phenobarbital to
• St John's wort, a herbal medicine
Repaglinide with food, drink and alcohol
Take Repaglinide before main meals.
Alcohol can alter the way this medicine works to
reduce your blood sugar levels. You should watch
for the signs or symptoms of hypo (low blood sugar
levels) if you consume alcohol.
Pregnancy and breast-feeding
You should not take repaglinide if you are pregnant
or you are planning to become pregnant.
REPAGLINIDE 0.5 mg
REPAGLINIDE 1 mg
REPAGLINIDE 2 mg
Package Leaflet: Information for the patient
See your doctor as soon as possible if you become
pregnant or are planning to become pregnant during
treatment. You should not take repaglinide if you
Ask your doctor or pharmacist for advice before
taking any medicine.
Driving and using machines
Your ability to drive or operate a machine may be
affected if your blood sugar is low or high. Bear in
mind that you could endanger yourself or others.
Please ask your doctor whether you can drive a car
• have frequent hypos
• have few or no warning signs of hypos.
3. HOW TO TAKE REPAGLINIDE
Always take this medicine exactly as your doctor
or pharmacist has told you. Do not take more
Repaglinide than your doctor has told you. Check
with your doctor or pharmacist for advice before
taking this medicine.
Your doctor will work out your dose.
• The normal starting dose is 0.5 mg before each
main meal. Swallow the tablets with a glass of water
immediately before or up to 30 minutes before
each main meal.
• The dose may be adjusted by your doctor by up
to 4 mg to be taken immediately before or up to
30 minutes before each main meal. The maximum
recommended daily dose is 16 mg.
Use in children and adolescents
Repaglinide is not recommended for children and
adolescents under 18 years of age.
If you take more Repaglinide than you should
If you take too many tablets your blood sugar
levels may become too low leading to hypo
(hypoglycaemia). Please see If you get a hypo (Section
2) on what a hypo is and how to treat it.
If you forget to take Repaglinide
Do not double the dose to make up for a forgotten
dose, take the next dose as usual.
If you stop taking Repaglinide
Be aware that the desired effect is not achieved if
you stop taking Repaglinide. Your diabetes may get
worse. If any change of your treatment is necessary
contact your doctor first.
If you have any further questions on the use of this
product, ask your doctor or pharmacist.
4. POSSIBLE SIDE EFFECTS
Like all medicines, this medicine can cause side
effects, although not everybody gets them.
Common side effects (may affect up to 1 in
• low blood sugar (Hypoglycaemia, see If you get a
hypo). The risk of getting a hypo may increase if you
take other medicines
• stomach pain
Rare side effects (may affect up to 1 in
• acute coronary syndrome (but it may not be due to
Very rare side effects (may affect up to 1 in
• allergy (such as swelling, difficulty breathing, rapid
heartbeat, feeling dizzy and sweating which could
be signs of anaphylactic reaction). Contact a
• visual disturbances
• severe liver problems including abnormal liver
function and raised liver enzymes in your blood
Reporting of side effects
If you get any of the side effects talk to your doctor
or pharmacist. This includes any possible side effects
not listed in this leaflet. You can also report side
effects directly via the Yellow Card System at:
www.mhra.gov.uk/yellowcard. By reporting side
effects you can help provide more information on
the safety of this medicine.
5. HOW TO STORE REPAGLINIDE
Keep this medicine out of the sight and reach
Do not use this medicine after the expiry date, which
is stated on the blister, carton or bottle label after
'EXP'. The expiry date refers to the last day of
Repaglinide supplied in HDPE bottle packs should be
used for no longer than 3 months after the bottle has
first been opened.
Do not use this medicine if you notice any
discolouration of tablets.
This medicinal product does not require any special
Do not throw away any medicines via wastewater or
household waste. Ask your pharmacist how to throw
away medicines you no longer use. These measures
will help protect the environment.
6. CONTENTS OF THE PACK AND
What Repaglinide contains:
• The active substance is repaglinide. Each tablet
contains 0.5 mg, 1 mg, and 2 mg of repaglinide.
• The other ingredients are:
* Povidone (PVP K-30)
* Sodium laurilsulphate
* Calcium hydrogen phosphate, anhydrous
* Cellulose, microcrystalline (E460)
* Maize starch
* Croscarmellose sodium
* Polacrilin potassium
* Magnesium stearate
* Silica, colloidal anhydrous
* Iron oxide yellow (E172) [1 mg tablets only]
* Iron oxide red (E172) [2 mg tablets only]
What Repaglinide looks like and contents of
The 0.5 mg tablets are white to off-white, round,
biconvex tablets debossed with 'M' on one side of
the tablet and 'R21' on the other side.
The 1 mg tablets are yellow, round, biconvex tablets
debossed with 'M' on one side of the tablet and 'R22'
on the other side.
The 2 mg tablets are peach-coloured, round,
biconvex tablets debossed with 'M' on one side of
the tablet and 'R23' on the other side.
The medicinal product is available in aluminium/
aluminium blister packs of 30, 90, 120, 180, 200 and
270 or bottles with a child resistant closure and
desiccant containing 120, 200 and 270 tablets
Not all pack sizes may be marketed.
Marketing Authorisation Holder
Mylan Hungary Kft.
Not known (cannot be estimated from the
• hypoglycaemic coma or unconsciousness (very
severe hypoglycaemic reactions – see If you get a
hypo). Contact a doctor immediately.
• feeling sick (nausea)
• hypersensitivity (such as rash, itchy skin, reddening
of the skin, swelling of the skin).
This leaflet was last approved in 02/2013
Source: Medicines and Healthcare Products Regulatory Agency
Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.