• Keep this leaflet. You may need to read it again.
• If you have any further questions, ask your doctor or pharmacist.
• This medicine has been prescribed for you only. 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.

1. What Atorvastatin is and what it is used for
2. What you need to know before you take Atorvastatin
3. How to take Atorvastatin
4. Possible side effects
5. How to store Atorvastatin
6. Contents of the pack and other information

• if you are allergic to atorvastatin or any of the other ingredients of this medicine (listed in section 6)
• if you have or have ever had a disease which affects the liver
• if you have had any unexplained abnormal blood tests for liver function
• if you are a woman able to have children and not using reliable contraception
• if you are pregnant or trying to become pregnant
• if you are breast-feeding.
• If you use the combination of glecaprevir/pibrentasvir in the treatment of hepatitis C

Talk to your doctor, pharmacist or nurse before taking Atorvastatin.

• if you have or have had myasthenia (a disease with general muscle weakness including in some cases muscles used when breathing), or ocular myasthenia (a disease causing eye muscle weakness) as statins may sometimes aggravate the condition or lead to the occurrence of myasthenia (see section 4).
• if you have severe respiratory failure
• if you are taking or have taken in the last 7 days a medicine called fusidic acid, (a medicine for bacterial infection) orally or by injection. The combination of fusidic acid and Atorvastatin can lead to serious muscle problems (rhabdomyolysis)
• if you have had a previous stroke with bleeding into the brain, or have small pockets of fluid in the brain from previous strokes
• if you have kidney problems
• if you have an under-active thyroid gland (hypothyroidism)
• if you have had repeated or unexplained muscle aches or pains, a personal history or family history of muscle problems
• if you have had previous muscular problems during treatment with other lipid-lowering medicines (e.g. other ‘-statin’ or ‘-fibrate’ medicines)
• if you regularly drink a large amount of alcohol
• if you have a history of liver disease
• if you are older than 70 years.

If any of these apply to you, your doctor will need to carry out a blood test before and possibly during your Atorvastatin treatment to predict your risk of muscle related side effects. The risk of muscle related side effects e.g rhabdomyolysis is known to increase when certain medicines are taken at the same time (see Section 2 “Other medicines and Atorvastatin”).

Also tell your doctor or pharmacist if you have a muscle weakness that is constant. Additional tests and medicines may be needed to diagnose and treat this.

While you are on this medicine your doctor will monitor you closely if you have diabetes or are at risk of developing diabetes. You are likely to be at risk of developing diabetes if you have high levels of sugars and fats in your blood, are overweight and have high blood pressure.

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.

There are some medicines that may change the effect of Atorvastatin or their effect may be changed by Atorvastatin. This type of interaction could make one or both of the medicines less effective.

Alternatively it could increase the risk or severity of side-effects, including the important muscle wasting condition known as rhabdomyolysis described in Section 4:

• Medicines used to alter the way your immune system works, e.g. ciclosporin
• Certain antibiotics or antifungal medicines, e.g. erythromycin, clarithromycin, telithromycin, ketoconazole, itraconazole, voriconazole, fluconazole, posaconazole, rifampin, fusidic acid
• Other medicines to regulate lipid levels, e.g. gemfibrozil, other fibrates, colestipol
• Some calcium channel blockers used for angina or high blood pressure, e.g. amlodipine, diltiazem,; medicines to regulate your heart rhythm e.g. digoxin, verapamil, amiodarone
• Letermovir, a medicine that helps stop you from getting ill from cytomegalovirus.
• Medicines used in the treatment of HIV e.g. ritonavir, lopinavir, atazanavir, indinavir, darunavir, the combination of tipranavir/ritonavir etc.
• Some medicines used in the treatment of hepatitis C e.g. telaprevir, boceprevir and the combination of elbasvir/grazoprevir, ledipasvir/sofosbuvir
• Other medicines known to interact with Atorvastatin include ezetimibe (which lowers cholesterol), warfarin (which reduces blood clotting), oral contraceptives, stiripentol (an anti-convulsant for epilepsy), cimetidine (used for heartburn and peptic ulcers), phenazone (a painkiller), colchicine (used to treat gout) and antacids (indigestion products containing aluminium or magnesium)
• Medicines obtained without a prescription: St John’s Wort
• If you need to take oral fusidic acid to treat a bacterial infection you will need to temporarily stop using this medicine. Your doctor will tell you when it is safe to restart Atorvastatin. Taking Atorvastatin with fusidic acid may rarely lead to muscle weakness, tenderness or pain (rhabdomyolysis). See more information regarding rhabdomyolysis in section 4
• Daptomycin (a medicine used to treat complicated skin and skin structure infections and bacteria present in the blood).

Tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription.

See Section 3 for instructions on how to take Atorvastatin. Please note the following:

Grapefruit juice

Do not take more than one or two small glasses of grapefruit juice per day because large quantities of grapefruit juice can change the effects of Atorvastatin.

Alcohol

Avoid drinking too much alcohol while taking this medicine. See Section 2 “Warnings and precautions” for details

Do not take Atorvastatin if you are pregnant, or if you are trying to become pregnant. Do not take Atorvastatin if you are able to become pregnant unless you use reliable contraceptive measures.

Do not take atorvastatin if you are breast-feeding

The safety of Atorvastatin during pregnancy and breast-feeding has not yet been proven. Ask your doctor or pharmacist for advice before taking any medicine.

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine

Normally this medicine does not affect your ability to drive or operate machines. However, do not drive if this medicine affects your ability to drive. Do not use any tools or machines if your ability to use them is affected by this medicine.

If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.

This medicine contains soya lecithin. If you are allergic to peanut or soya, do not take this medicinal product.

This medicine contains less than 1 mmol of sodium (23 mg) per tablet, that is to say essentially ‘sodium-free.’

Please ask your doctor if you think that the effect of Atorvastatin is too strong or too weak.

If you accidently take too many Atorvastatin tablets (more than your usual daily dose), contact your doctor or nearest hospital for advice.

If you forget to take a dose, just take your next scheduled dose at the correct time. Do not take a double dose to make up for a forgotten dose.

If you have any further questions on the use of this medicine or wish to stop your treatment, ask your doctor or pharmacist.

Common (may affect up to 1 in 10 people):

• inflammation of the nasal passages, pain in the throat, nose bleed
• allergic reactions
• increases in blood sugar levels (if you have diabetes continue careful monitoring of your blood sugar levels), increase in blood creatine kinase
• headache
• nausea, constipation, wind, indigestion, diarrhoea
• joint pain, muscle pain and back pain
• blood test results that show your liver function can become abnormal

Uncommon (may affect up to 1 in 100 people):

• anorexia (loss of appetite), weight gain, decreases in blood sugar levels (if you have diabetes you should continue careful monitoring of your blood sugar levels)
• having nightmares, insomnia
• dizziness, numbness or tingling in the fingers and toes, reductions of sensation to pain or touch, change in sense of taste, loss of memory
• blurred vision
• ringing in the ears and/or head
• vomiting, belching, abdominal pain upper and lower, pancreatitis (inflammation of the pancreas leading to stomach pain)
• hepatitis (liver inflammation)
• rash, skin rash and itching, hives, hair loss
• neck pain, muscle fatigue
• fatigue, feeling unwell, weakness, chest pain, swelling especially in the ankles (oedema), raised temperature
• urine tests that are positive for white blood cells

Rare (may affect up to 1 in 1,000 people):

• visual disturbance
• unexpected bleeding or bruising
• cholestasis (yellowing of the skin and whites of the eyes)
• tendon injury
• rash that may occur on the skin or sores in the mouth (lichenoid drug reaction)
• purple skin lesions (signs of blood vessel inflammation, vasculitis)

Very rare (may affect up to 1 in 10,000 people):

• an allergic reaction - symptoms may include sudden wheezing and chest pain or tightness, swelling of the eyelids, face, lips, mouth, tongue or throat, difficulty breathing, collapse
• hearing loss
• gynecomastia (breast enlargement in men).

Not known (frequency cannot be estimated from the available data):

• Muscle weakness that is constant.
• Myasthenia gravis (a disease causing general muscle weakness including in some cases muscles used when breathing).
• Ocular myasthenia (a disease causing eye muscle weakness).

Talk to your doctor if you experience weakness in your arms or legs that worsens after periods of activity, double vision or drooping of your eyelids, difficulty swallowing, or shortness of breath.

• Sexual difficulties
• Depression
• Breathing problems including persistent cough and/or shortness of breath or fever
• Diabetes. This is more likely if you have high levels of sugars and fats in your blood, are overweight and have high blood pressure. Your doctor will monitor you while you are taking this medicine.

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly (see details below). By reporting side effects you can help provide more information on the safety of this medicine.

The United Kingdom

or search for MHRA Yellow Card in the Google Play or Apple App Store.

For 10 mg, 20 mg, 30 mg, 40 mg, 60 mg and 80 mg (PA/Al/PVC-Al):

This medicine does not require any special storage conditions.

For 10 mg and 20 mg (PVC/PE/PVdC/ Al):

This medicine does not require any special storage conditions.

For 40 mg and 80 mg (PVC/PE/PVdC-Al):

Store below 30 ºC

This medicine does not require any special storage conditions

Use within 9 months after first opening the HDPE container.

Do not use this medicine after the expiry date which is stated on the label, carton and blister after EXP. The expiry date refers to the last day of that month.

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.

• The active substance is atorvastatin
  Each film coated tablet contains 10 mg atorvastatin (as atorvastatin calcium trihydrate).
  Each film coated tablet contains 20 mg atorvastatin (as atorvastatin calcium trihydrate).
  Each film coated tablet contains 30 mg atorvastatin (as atorvastatin calcium trihydrate).
  Each film coated tablet contains 40 mg atorvastatin (as atorvastatin calcium trihydrate).
  Each film coated tablet contains 60 mg atorvastatin (as atorvastatin calcium trihydrate).
  Each film coated tablet contains 80 mg atorvastatin (as atorvastatin calcium trihydrate).
• The other ingredients are.
  Tablet core: Mannitol, copovidone, sodium carbonate (E500), croscarmellose sodium (E468), silicified microcrystalline cellulose (E460) (contains Silica, colloidal anhydrous and microcrystalline cellulose), lactose monohydrate, sodium lauryl sulfate, silica colloidal anhydrous, magnesium stearate (E572).
  Tablet coat (Ready to use coating material): Poly vinyl alcohol – part hydrolyzed, titanium dioxide (E171), talc (E553b), lecithin (soya) (E322), xanthan gum (E415).

Film-coated tablet

Atorvastatin 10 mg film-coated tablets

White, elliptical [9.8 mm x 5.2 mm], film-coated tablets, debossed with “AS” on one side and “10” on other side.

Atorvastatin 20 mg film-coated tablets

White, elliptical [12.3 mm x 6.5 mm], film-coated tablets, debossed with “AS” on one side and “20” on other side.

Atorvastatin 30 mg film-coated tablets

White, round [10.1 mm], film coated tablets, debossed with “N” on one side and “30” on other side.

Atorvastatin 40 mg film-coated tablets

White, elliptical [15.5 mm x 8.1 mm], film-coated tablets, debossed with “AS” on one side and “40” on other side.

Atorvastatin 60 mg film-coated tablets

White, oval [17.6 mm x 9.3 mm], film coated tablets, debossed with “N” on one side and “60” on other side.

Atorvastatin 80 mg film-coated tablets

White, elliptical [19.4 mm x 10.4 mm], film-coated tablets, debossed with “AS” on one side and “80” on other side.

For 10 mg, 20 mg, 30 mg, 40 mg, 60 mg and 80 mg:

Atorvastatin film-coated tablets are available in polyamide/ Aluminium foil/ PVC - Aluminium foil blisters packs and HDPE bottle packs with polypropylene closure. Bottle pack contains silica gel as desiccant.

For 10 mg, 20 mg, 40 mg and 80 mg:

Atorvastatin film-coated tablets are also available in PVC/PE/PVdC- Aluminium foil blister as alternate blister pack.

Pack sizes:

Blister pack

For 10 mg, 20 mg, 40 mg and 80 mg: 14, 28, 30, 50, 56, 90, 100 and 500 film-coated tablets

For 30 mg and 60 mg: 28, 30, 50, 60, 100 film-coated tablets.

HDPE bottle pack:

30, 90, 100, 200 and 250 film-coated tablets (for 10 mg, 20 mg and 40 mg) 30 and 200 film-coated tablets (for 80 mg).

Not all pack sizes may be marketed.

For 10 mg, 20 mg, 30 mg, 40 mg, 60 mg, 80 mg:

or

or