Patient Information Leaflet
Safinamide Cinfa 50 mg film-coated tablets EFG
Safinamide Cinfa 100 mg film-coated tablets EFG
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
Safinamide Cinfa is a medicine whose active substance is safinamide. It works to increase the level of a substance called dopamine in the brain, which is involved in controlling movement and is present in reduced amounts in the brain of patients with Parkinson's disease. Safinamide is used to treat Parkinson's disease in adults.
In patients in the mid-to-advanced stage of the disease, who experience sudden changes between "ON" (with the ability to move) and "OFF" (with difficulty moving), safinamide is added to a stable dose of the medicine called levodopa alone or in combination with other medicines for Parkinson's disease.
Do not take Safinamide Cinfa
You must wait at least 7 days between stopping treatment with safinamide before starting treatment with MAOIs or pethidine.
Warnings and precautions
Consult your doctor before starting to take safinamide:
Children and adolescents
Safinamide is not recommended for use in children and adolescents under 18 years of age due to lack of data on safety and efficacy in this population.
Other medicines and Safinamide Cinfa
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines. Consult your doctor before taking the following medicines with safinamide:
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor for advice before taking this medicine.
Pregnancy
Safinamide should not be used during pregnancy or in women of childbearing potential not using adequate contraception.
Breastfeeding
It is likely that safinamide passes into breast milk. Safinamide should not be used during breastfeeding.
Driving and using machines
During treatment with safinamide, drowsiness and dizziness may occur; patients should be cautious when using hazardous machinery or driving until they are sure that safinamide does not affect them in any way.
Consult your doctor before driving or using machines.
Follow exactly the administration instructions of this medicine given by your doctor. If you are unsure, consult your doctor again.
The recommended starting dose of safinamide is one 50 mg tablet, which can be increased to one 100 mg tablet, once daily, preferably in the morning, orally with water. Safinamide can be taken with or without food.
If you have moderate liver impairment, you should not take more than 50 mg per day. Your doctor will confirm if this is the case for you.
If you take more Safinamide Cinfa than you should
If you have taken too many safinamide tablets, you may develop high blood pressure, anxiety, confusion, inattention, drowsiness, dizziness, feel nauseous, or vomit, have dilated pupils, or develop involuntary muscle contractions. Contact your doctor immediately and take the safinamide packaging with you.
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 medicine and the amount taken.
If you forget to take Safinamide Cinfa
Do not take a double dose to make up for forgotten doses. Skip that dose and take the next dose when you normally take it.
If you stop taking Safinamide Cinfa
Do not stop taking safinamide without consulting your doctor first.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Seek medical attention in case of hypertensive crisis (very high blood pressure, collapse), malignant neuroleptic syndrome (confusion, sweating, hypertonia, hyperthermia, increased creatine kinase levels in the blood), serotonin syndrome (confusion, hypertension, muscle rigidity, hallucinations), and hypotension.
The following side effects have been reported in patients with Parkinson's disease in the mid-to-advanced stage (patients taking safinamide as an add-on to levodopa alone or in combination with other Parkinson's disease medicines):
Common(may affect up to 1 in 10 people): insomnia, difficulty performing voluntary movements, feeling of sleep, dizziness, headache, worsening of Parkinson's disease, cataract, low blood pressure when standing up, nausea, and falls.
Uncommon(may affect up to 1 in 100 people): urinary tract infection, skin cancer, low iron levels in the blood, low white blood cell count, alteration of red blood cells, decreased appetite, high fat levels in the blood, increased appetite, high blood sugar levels, seeing things that are not there, feeling sad, abnormal dreams, fear and anxiety, confusion, mood changes, increased interest in sex, abnormal perceptions and thoughts, agitation, sleep disorder, numbness, instability, loss of sensitivity, prolonged abnormal muscle contraction, headache, difficulty speaking, fainting, memory impairment, blurred vision, blind spot, double vision, sensitivity to light, disorders of the light-sensitive layer at the back of the eye, eye redness, increased eye pressure, feeling that the room is spinning, feeling heartbeats, rapid heartbeats, irregular heartbeats, slow heartbeats, high blood pressure, low blood pressure, enlarged and twisted veins, cough, difficulty breathing, nasal discharge, constipation, heartburn, vomiting, dry mouth, diarrhea, abdominal pain, stomach upset, gas, feeling full, drooling, mouth ulcers, sweating, itching, sensitivity to light, skin redness, back pain, joint pain, muscle cramps, stiffness, pain in arms or legs, muscle weakness, feeling heavy, increased urination at night, pain when urinating, difficulty urinating, prostate problems, breast pain, decreased drug effect, drug intolerance, feeling cold, feeling unwell, fever, dryness of the skin, eyes, or mouth, abnormal blood tests, heart murmur, abnormal heart tests, bruising or swelling after injury, blockage of blood vessels due to fat, head trauma, mouth injuries, skeletal injuries, gambling.
Rare(may affect up to 1 in 1,000 people): pneumonia, skin infection, sore throat, nasal allergy, dental infection, viral infection, non-cancerous skin growths/disorders, white blood cell abnormalities, severe weight loss and weakness, high potassium levels in the blood, uncontrolled impulses, stupor, disorientation, incorrect image perception, decreased interest in sex, thoughts that cannot be shaken, feeling of being pursued, premature ejaculation, uncontrollable need to sleep, fear of social situations, suicidal thoughts, clumsiness, ease of distraction, loss of sense of taste, weak or slow reflexes, pain in the legs that radiates, constant urge to move the legs, feeling of sleep, eye abnormalities, progressive vision loss due to diabetes, increased tearing, night blindness, crossed eyes, heart attack, blood vessel contraction or narrowing, very high blood pressure, chest tightness, difficulty speaking, difficulty or pain when swallowing, gastroduodenal ulcer, nausea, stomach bleeding, jaundice, hair loss, blistering, skin allergy, skin disorders, bruising, scaly skin, night sweats, skin pain, skin discoloration, psoriasis, flaky skin, inflammation of the spine joints due to an autoimmune disease, back pain, joint inflammation, musculoskeletal pain, muscle pain, neck pain, joint pain, joint cyst, uncontrollable need to urinate, increased urination, pus in the urine, difficulty urinating, prostate problems, breast pain, decreased drug effect, drug intolerance, feeling cold, feeling unwell, fever, dryness of the skin, eyes, or mouth, abnormal blood tests, heart murmur, abnormal heart tests, bruising or swelling after injury, blockage of blood vessels due to fat, head trauma, mouth injuries, skeletal injuries, gambling.
Reporting of side effects
If you experience any 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 to the Spanish Medicines and Healthcare Products Agency via their website: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton and blister after "EXP".
The expiry date refers to the last day of the month stated.
This medicine does not require any special storage conditions.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Composition of Safinamide Cinfa
Appearance of the product and pack contents
Safinamide Cinfa 50 mg are orange, round, film-coated tablets with a metallic sheen, engraved with "MS" on one side and "18" on the other side.
Safinamide Cinfa 100 mg are orange, round, film-coated tablets with a metallic sheen, engraved with "MS" on one side and "19" on the other side.
Safinamide Cinfa is available in blisters containing 14, 28, 30, 90, or 100 film-coated tablets.
Not all pack sizes may be marketed.
Marketing authorisation holder and manufacturer
Marketing authorisation holder
Laboratorios Cinfa, S.A.
Carretera Olaz-Chipi, 10. Polígono Industrial Areta
31620 Huarte (Navarra)
Spain
Manufacturer
MSN Labs Europe Limited,
KW20A Corradino Park,
Paola, PLA 3000,
Malta
Or
Pharmadox Healthcare Limited,
KW20A Kordin Industrial Park,
Paola, PLA 3000,
Malta
This medicine is authorised in the Member States of the European Economic Area under the following names:
Spain: Safinamide Cinfa 50 mg film-coated tablets EFG
Safinamide Cinfa 100 mg film-coated tablets EFG
Germany: Safinamid Vivanta Generics 50 mg film-coated tablets
Safinamid Vivanta Generics 100 mg film-coated tablets
Date of last revision of this leaflet: March 2025
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Healthcare Products (AEMPS) http://www.aemps.gob.es/