PRAVASTATIN TEVA-RATIO 10 mg TABLETS

2. What you need to know before taking Pravastatina Teva-ratio

Do not take Pravastatina:

• If you are allergic to pravastatin or any of the other components of this medication (listed in section 6).
• If you are pregnant, plan to become pregnant, or are breastfeeding (see Pregnancy and breastfeeding).
• If you have active liver disease (liver disease).
• If several blood tests show abnormal liver function (elevated liver enzyme levels in the blood)

Warnings and precautions

Before taking this treatment, you should consult your doctor if you have or have had any of the following medical problems:

• Kidney disease
• Decreased thyroid gland activity (hypothyroidism)
• Liver disease or alcohol-related problems (drinking large amounts of alcohol)
• Muscle disorders caused by a hereditary disease
• Muscle problems caused by another medication belonging to the group of statins (HMG-CoA reductase inhibitors) or belonging to the group known as fibrates (see Use of other medications).
• If you have or have had myasthenia (a disease characterized by generalized muscle weakness that, in some cases, affects the muscles used for breathing) or ocular myasthenia (a disease that causes weakness of the eye muscles), as statins can sometimes worsen the disease or cause myasthenia to appear (see section 4).

Your doctor will perform a blood test before starting Pravastatina and if you have any symptoms or liver problems during treatment. This is to check if your liver is functioning properly.

Your doctor may also need to perform a blood test after starting Pravastatina to check liver function.

The risk of muscle failure is higher in some patients. Consult your doctor in the following cases:

If you are taking or have taken orally or by injection a medication called fusidic acid (an antibiotic) in the last 7 days, combining it with Pravastatina can cause serious muscle problems (rhabdomyolysis).

If you have had any of these problems or are over 70 years old, your doctor will perform a blood test before and probably during treatment. These blood tests will be used to assess the risk of you experiencing muscle side effects.

If you experience unexplained muscle cramps or pain during treatment, inform your doctor immediately.

If you have diabetes or are at risk of developing it, your doctor will closely monitor you during treatment with this medication. You are likely to be at risk of developing diabetes if you have high blood sugar and fat levels, are overweight, and have hypertension.

Also, inform your doctor or pharmacist if you experience constant muscle weakness. Additional tests and medications may be necessary to diagnose and treat this problem.

Consult your doctor before taking Pravastatina.

Consult your doctor or pharmacist before taking Pravastatina if you:

• Have severe respiratory failure.

Other medications and Pravastatina

Inform your doctor or pharmacist if you are taking, have recently taken, or may need to take any other medication.

Taking Pravastatina with any of the following medications can increase the risk of muscle problems:

• A medication that lowers cholesterol levels in the blood (fibrates, e.g., gemfibrozil, fenofibrate).
• A medication that weakens the body's immune system (cyclosporin).
• An antibiotic used to treat bacterial infections (e.g., erythromycin or clarithromycin).
• If you need to take fusidic acid orally to treat a bacterial infection, you will need to temporarily stop taking this medication. Your doctor will indicate when it is safe to restart Pravastatina treatment. Taking Pravastatina with fusidic acid can rarely cause muscle weakness, sensitivity, or pain (rhabdomyolysis). See more information on rhabdomyolysis in section 4.
• Colchicine (a medication used to treat gout)
• Nicotinic acid (a medication used to lower high cholesterol levels in the blood)
• Rifampicin (a medication used to treat tuberculosis)
• Lenalidomide (a medication used to treat a type of blood cancer called multiple myeloma).
• If you are taking a medication used to treat and prevent blood clots called "vitamin K antagonist," inform your doctor before taking pravastatin, as the use of vitamin K antagonists in combination with pravastatin may increase the results of blood tests used to monitor treatment with vitamin K antagonists.
• If you are also using a medication to lower fat levels in your blood (such as resin-like cholestyramine or colestipol), this treatment should be taken at least one hour before or four hours after taking the resin. This is because the resin can affect the absorption of Pravastatina if these two medications are taken simultaneously.

Taking Pravastatina with food and drinks

This treatment can be taken with or without food, with a half glass of water.

You should minimize your alcohol consumption. If you have doubts about how much alcohol you can drink while taking this medication, you should consult your doctor.

Pregnancy and breastfeeding

Do not take Pravastatina during pregnancy. If you discover that you are pregnant, you should inform your doctor immediately.

Consult your doctor or pharmacist before using any medication.

Do not take Pravastatina during breastfeeding, as this treatment passes into breast milk.

Driving and using machines

Pravastatina normally does not affect your ability to drive or use machines. However, if you notice symptoms of dizziness, blurred vision, or double vision during treatment, do not drive or use machines until you are sure you can do so safely.

Pravastatina Teva-ratio contains lactose and sodium

If your doctor has told you that you have an intolerance to certain sugars, consult with them before taking this medication.

This medication contains less than 1 mmol of sodium (23 mg) per tablet; this is essentially "sodium-free."

3. How to take Pravastatina Teva-ratio

Follow the administration instructions for this medication exactly as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.

Your doctor will advise you on a low-fat diet, which you should continue until the end of treatment.

Pravastatina can be taken with or without food, with a half glass of water.

The recommended dose is:

Adults

• In the treatment of high cholesterol and fat levels in the blood: the normal dose is 10-40 mg once a day, preferably at night.
• In the prevention of heart and blood vessel diseases: the normal dose is 40 mg once a day, preferably at night.

Do not exceed the maximum daily dose of 40 mg of pravastatin. Your doctor will determine the appropriate dose for you.

Children (8-13 years) and adolescents (14-18 years) with a hereditary disease that increases cholesterol levels in the blood:

The recommended dose between 8 and 13 years is 10-20 mg once a day, and the recommended dose between 14 and 18 years is 10-40 mg once a day.

After an organ transplant:

Your doctor may prescribe an initial dose of 20 mg once a day. Your doctor may adjust the dose up to 40 mg.

If you are also taking a medication that weakens the body's immune system (cyclosporin), your doctor may prescribe an initial dose of 20 mg once a day. This dose may be adjusted up to 40 mg by your doctor.

If you have severe kidney or liver disease, your doctor may prescribe a lower dose of Pravastatina.

If you think the action of this treatment is too strong or too weak, inform your doctor or pharmacist.

Duration of treatment

Your doctor will indicate the duration of your treatment with pravastatin. This medication should be taken regularly for the time recommended by your doctor, even if it is for a long period. Do not stop treatment on your own.

If you take more Pravastatina than you should

If you have taken more Pravastatina than you should, or if someone has accidentally swallowed some tablets, contact your doctor or pharmacist or the nearest hospital.

In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medication and the amount ingested.

If you forget to take Pravastatina

If you forget to take a dose, simply take your normal dose when the next one is due.

Do not take a double dose to make up for forgotten doses.

If you have any other questions about the use of this product, ask your doctor or pharmacist.

4. Possible side effects

Like all medications, this medication can cause side effects, although not everyone will experience them.

Stop taking Pravastatina and inform your doctor immediatelyif you notice unexplained or persistent muscle pain, pain on palpation, weakness, or cramps, especially if you do not feel well or have a fever.

In very rare cases, muscle problems can be serious (rhabdomyolysis) and can cause a life-threatening kidney disease.

Serious and sudden allergic reactions such as swelling of the face, lips, tongue, or trachea can cause serious breathing difficulties. This is a very rare reaction that can be serious if it occurs. You should inform your doctor immediately if this happens.

The following side effects are uncommon and may affect up to 1 in 100 people:

• Nervous system disorders: dizziness, fatigue, headache, sleep disorders, including insomnia.
• Eye disorders: blurred vision or double vision.
• Gastrointestinal disorders: indigestion, nausea, vomiting, stomach pain or discomfort, diarrhea, constipation, and gas.
• Skin and hair disorders: itching, acne, rash, blistering accompanied by itching, hair and scalp abnormalities (including hair loss).
• Urinary and genital disorders: changes in urine elimination (such as pain when urinating, frequent urination, or increased urination at night) and sexual problems.
• Muscle and joint disorders: muscle and joint pain, tendon inflammation that can be complicated by tendon rupture.

The following side effects are rare and may affect up to 1 in 1,000 people:

• Sensitivity to sunlight.

The following side effects are very rare and may affect up to 1 in 10,000 people:

• Nervous system disorders: alterations in touch sensation, including burning or tingling, or numbness, which indicates nerve damage.
• Skin disorders: severe skin alteration (lupus-like syndrome).
• Liver disorders: liver or pancreas inflammation, jaundice (recognized by yellowing of the skin and whites of the eyes), rapid destruction of liver cells (fulminant hepatic necrosis).
• Muscle and bone disorders: inflammation of one or more muscles causing pain or muscle weakness (myositis or polymyositis or dermatomyositis), pain or weakness in muscles, tendon inflammation, sometimes complicated by rupture.
• Altered blood tests: increased transaminases (a group of blood enzymes) that may indicate liver problems. Your doctor may want to perform periodic tests to monitor this.

If you think any of the side effects you are experiencing is serious or if you notice any side effect not mentioned in this package leaflet, inform your doctor or pharmacist.

Possible side effects

• Nightmares
• Memory loss
• Depression
• Respiratory problems, including persistent cough and/or difficulty breathing or fever.
• Diabetes: it is more likely if you have high blood sugar and fat levels, are overweight, and have hypertension. Your doctor will monitor you during treatment with this medication.

Side effects of unknown frequency: constant muscle weakness, liver failure, muscle rupture.

Severe myasthenia (a disease that causes generalized muscle weakness that, in some cases, affects the muscles used for breathing).

Ocular myasthenia (a disease that causes weakness of the eye muscles).

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

Reporting side effects

If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect not listed in this package leaflet. You can also report them directly through the Spanish Pharmacovigilance System for Human Use https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medication.

5. Storage of Pravastatina Teva-ratio

Keep this medication out of sight and reach of children.

Do not use this medication after the expiration date shown on the packaging after CAD. The expiration date is the last day of the month indicated.

Do not store above 30 ºC. Keep in the original packaging to protect it from moisture.

Medications should not be disposed of through wastewater or household waste. Deposit the packaging and medications you no longer need at the SIGRE point in the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.

6. Packaging Content and Additional Information

Composition of Pravastatina Teva-ratio 10 mg

• The active ingredient is pravastatin sodium. Each tablet contains 10 mg of pravastatin sodium.

sodium.

• The other components are: lactose, povidone (PVP K-30), crospovidone, calcium hydrogen phosphate (E341), sodium stearyl fumarate, microcrystalline cellulose (E460), sodium croscarmellose (E466), red iron oxide (E172).

Appearance of the Product and Packaging Content

• Tablet.
• Round, speckled, pink tablets, slightly convex, scored on both sides. The tablet can be divided into equal doses.
• Pravastatina Teva-ratio 10 mg is available in pack sizes of 20, 28, 30, 50, 60, 84, 90, and 100 tablets and clinical packs of 50 tablets in unit doses.

Marketing Authorization Holder and Manufacturer:

Marketing Authorization Holder:

Teva Pharma, S.L.U.

Anabel Segura Street, 11. Albatros B Building, 1st Floor.

28108 Alcobendas (Madrid).

Manufacturer:

Pharmachemie B.V,

Swensweg 5, Postbox 552,

2003 RN Haarlem

Netherlands

or

Teva Pharmaceutical Works Private Ltd. Co.,

Pallagi Street 13, 4042 Debrecen

Hungary

or

Teva Czech Industries s.r.o.,

Ostravská 29, c.p. 305, 747 70

Opava–Komárov, Czech Republic

or

Teva Pharma S.L.U.,

Malpica Industrial Park, Street C, No. 4,

50016 Zaragoza, Spain

or

Merckle GmbH,

Ludwig-Merckle-Str. 3,

89143 Blaubeuren, Germany

This medicinal product is registered in the EEA Member States with the following names:

Germany: Pravastatin-ratiopharm 10 mg Tablets

Netherlands: Pravastatin sodium ratiopharm 10 mg Teva, tablets

Portugal: Pravastatina ratiopharm 10mg Tablets

Spain: Pravastatina Teva-ratio 10 mg tablets EFG

Date of the Last Revision of this Leaflet:April 2023

“Detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/”

You can access detailed and updated information about this medicinal product by scanning the QR code included in the packaging with your mobile phone (smartphone). You can also access this information at the following internet address: https://cima.aemps.es/cima/dochtml/p/74544/P_74544.html