


Ask a doctor about a prescription for QUINAPRIL NORMON 40 mg FILM-COATED TABLETS
Package Leaflet: Information for the User
Quinapril Normon 40 mg Film-Coated Tablets EFG
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.
Contents of the pack and other information
Quinapril belongs to a group of medicines called angiotensin-converting enzyme inhibitors (ACE inhibitors). It works by widening the blood vessels, making it easier for the heart to pump blood to all parts of the body and helping to reduce high blood pressure.
Your doctor has prescribed quinapril for the treatment of:
Treatment with Quinapril Normon requires regular monitoring by your doctor.
Do not take Quinapril Normon
Warnings and precautions
Talk to your doctor or pharmacist before starting Quinapril Normon:
Talk to your doctor if you experience dizziness and vertigo. If dizziness occurs, lie down until the sensation passes. After being in bed, always get up slowly to avoid the sensation of dizziness. If you faint or feel dizzy, inform your doctor.
As with other ACE inhibitors, dry cough may occur when taking Quinapril Normon, which disappears when treatment is stopped. In this case, consult your doctor.
Talk to your doctor if any of the above circumstances have ever occurred to you.
Your doctor may monitor your kidney function, blood pressure, and blood electrolyte levels (e.g., potassium) at regular intervals.
See also the information under the heading "Do not take Quinapril Normon".
Talk to your doctor or pharmacist before taking any medicine.
Patients over 65 years old
If you are elderly, you may be more sensitive to the effects mentioned above. If any of these effects occur, inform your doctor immediately.
Using Quinapril Normon with other medicines
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines, including those obtained without a prescription.
Your doctor may need to change your dose and/or take other precautions:
If you are taking an angiotensin II receptor antagonist (ARA) or aliskiren (see also the information under the headings "Do not take Quinapril Normon" and "Warnings and precautions").
If you are hospitalized or visit another doctor, dentist, or pharmacist, inform them that you are taking Quinapril Normon or any other medicine. Inform your doctor that you are receiving treatment with Quinapril Normon if you are going to undergo any surgical procedure.
Quinapril Normon may interact with the following medicines. It is especially important that you inform your doctor if you are taking:
If you have any doubts about taking other medicines with Quinapril Normon, consult your doctor.
Using Quinapril Normon with food and drink
Quinapril Normon can be taken with or without food.
Pregnancy, breastfeeding, and fertility
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:
Inform your doctor if you think you are or might be pregnant. Normally, your doctor will advise you to stop taking Quinapril Normon before you become pregnant or as soon as you know you are pregnant and will advise you to take another medicine instead of Quinapril Normon. Quinapril Normon is not recommended at the beginning of pregnancy and should not be taken after the third month of pregnancy, as it can cause serious harm to your baby if used after the third month of pregnancy.
Breastfeeding
Ask your doctor or pharmacist for advice before taking any medicine.
Tell your doctor if you are breastfeeding or about to start breastfeeding. It is not recommended to take this medicine during breastfeeding in newborns (first weeks after birth) and especially in premature babies. In the case of older babies, your doctor will advise you on the benefits and risks of administering this medicine during breastfeeding, compared to other treatments.
Driving and using machines
Quinapril Normon may cause a sudden drop in blood pressure, leading to dizziness and, in some cases, fainting. This can occur especially during the first days of treatment. Therefore, at the beginning of treatment, do not perform tasks that require special attention (e.g., driving a car or operating hazardous machinery) until you know how you tolerate the treatment.
Follow exactly the administration instructions of this medicine given by your doctor. If you are unsure, consult your doctor again.
Remember to take your medicine.
Your doctor will indicate the duration of your treatment with Quinapril Normon. Your doctor may increase or decrease the dose if necessary until the dose that you need is found. Do not stop treatment before, as it may increase your blood pressure or worsen your heart function.
This treatment has been indicated by your doctor specifically for you and your disease. The dose will be established by the doctor according to the needs of each patient. Depending on the individual response, the doctor may modify the quinapril dosage. Follow your doctor's instructions faithfully regarding the dose and method of use.
Quinapril is administered orally. Your doctor will indicate how many tablets you should take each day.
Use in children:the safety and efficacy of quinapril in children have not been established. It should not be administered to children without consulting a doctor.
Instructions for the correct use of the medicine
The Quinapril Normon 40 mg tablet is administered orally and should be swallowed without chewing. Take the tablets with a sufficient amount of liquid (a glass of water). It can be taken with or without food.
If you think the effect of this medicine is too strong or too weak, do not change the dose yourself and inform your doctor or pharmacist.
If you take more Quinapril Normon than you should
In case of overdose or accidental ingestion, consult your doctor or the Toxicology Information Service, Telephone 91 562 04 20. Bring this leaflet with you.
The most likely symptom that would be expected after an overdose of quinapril would be a drop in blood pressure. Symptomatic treatment will be performed, compensating for the effects of this medicine.
In severe cases, the necessary measures will be taken; in addition to maintaining blood volume, it may be necessary to administer medicines that restore blood pressure adequately.
If you forget to take Quinapril Normon
Do not take a double dose to make up for forgotten doses.
If you have any other doubts about the use of this medicine, ask your doctor or pharmacist.
If you stop taking Quinapril Normon
Your doctor will indicate the duration of your treatment with Quinapril Normon. Do not stop taking Quinapril Normon without consulting your doctor. Normally, medicines for treating high blood pressure or heart failure should be taken for life. If you stop taking Quinapril Normon, your condition may worsen.
If you have any other doubts about the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause adverse effects, although not all people suffer from them.
The adverse reactions of quinapril vary in intensity from one individual to another, and should be taken into account especially at the start of treatment, when modifying the dose or when changing medication.
Stop taking Quinapril Normon and contact your doctor immediately if:
The following are the possible adverse effects during treatment with Quinapril Normon, according to their frequency.
Common adverse effects(may affect between 1 and 10 people out of 100)are: Headache, dizziness, inflammation of the nasal mucosa (rhinitis), cough, fatigue, weakness (asthenia), nausea and/or vomiting, muscle pain (myalgia), diarrhea, chest pain, abdominal pain, digestive discomfort (dyspepsia), breathing difficulties (dyspnea), back pain, pharynx inflammation (pharyngitis), difficulty falling asleep (insomnia), higher than normal levels of certain substances in blood tests (potassium, creatinine, and ureic nitrogen), decreased sodium concentrations in blood, low blood pressure (hypotension), and tingling (paresthesia).
Uncommon adverse effects (may affect between 1 and 10 people out of 1,000)are: Palpitations, dilation of blood vessels (vasodilation), oppressive chest pain (angina pectoris), increased heart rate (tachycardia), myocardial infarction, flatulence, dryness of the mouth or throat, depression, nervousness, confusion, somnolence, temporary interruption of blood supply to an area of the brain (transient ischemic attacks), dizziness, ringing in the ears, sinus inflammation (sinusitis), upper respiratory tract infection, bronchial inflammation (bronchitis), allergic reaction with swelling of the face, tongue, or throat that can cause breathing difficulties (angioedema), urinary tract infections, altered kidney function, protein in the urine, impotence, decreased visual acuity (amblyopia), fever, and excessive fluid accumulation in the body (edema).
Rare adverse effects (may affect up to 1 person out of 1,000)are: Balance disorder, fainting, respiratory disorder (eosinophilic pneumonia), taste alteration, constipation, tongue inflammation, hives, and various skin lesions that can be severe (erythema multiforme, pemphigus).
Very rare adverse effects (may affect up to 1 person out of 10,000)are: Blurred vision, intestinal obstruction (ileus), inflammation in the intestinal tract (intestinal angioedema), and skin eruption like psoriasis.
Adverse effects with unknown frequency(cannot be estimated from the available data) are: Decrease in the number of white blood cells that can favor infections (agranulocytosis), decrease in the number of red blood cells (anemia), decrease in the number of a type of white blood cells (neutropenia), decrease in the number of platelets (thrombocytopenia), severe allergic reaction (anaphylactoid reaction), dark urine, nausea, vomiting, muscle cramps, confusion, and convulsions. These may be symptoms of a condition called SIADH (inadequate secretion of antidiuretic hormone), stroke, decrease in blood pressure when standing up that can cause dizziness (postural hypotension), bronchial constriction that prevents breathing (bronchospasm), in individual cases, obstruction of the upper airways by angioedema (which can be fatal), pancreas inflammation (pancreatitis), liver inflammation (hepatitis), jaundice (cholestatic jaundice), severe skin disease with blistering and skin loss (necrotizing epidermolysis), various skin lesions that can be severe (exfoliative dermatitis, Stevens-Johnson syndrome), hair loss (alopecia), sensitivity to sunlight (photosensitivity), inflammation of serous tissues, skin changes associated with fever, muscle and joint pain (myalgia, arthralgia, arthritis), blood vessel inflammation (vasculitis), certain changes in blood test values (eosinophilia, leukocytosis, and/or elevated levels of antinuclear antibodies and erythrocyte sedimentation rate), psoriasis or worsening of existing psoriasis (skin disease characterized by red plaques covered with silver scales), reduction of hematocrit, reduction of hemoglobin, and elevation of liver enzymes and bilirubin. In some patients who have a congenital enzyme deficiency (glucose-6-phosphate dehydrogenase deficiency), cases of anemia due to red blood cell destruction (hemolytic anemia) have been reported.
Reporting of Adverse Effects
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect that is not listed in this leaflet. You can also report them directly through the Spanish Medicines and Healthcare Products Agency's pharmacovigilance system: https://www.notificaram.es. By reporting adverse effects, you can contribute to providing 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 expiration date stated on the packaging after CAD. The expiration date is the last day of the month indicated.
Store below 30°C.
Medicines should not be disposed of via wastewater or household waste. Deposit the packaging and medicines you no longer need at the SIGRE point in your pharmacy. In case of doubt, ask your pharmacist how to dispose of the packaging and medicines you no longer need. This way, you will help protect the environment.
Composition of Quinapril Normon 40 mg film-coated tablets EFG
Appearance of the Product and Package Contents
Brown, round, biconvex tablets.
The tablets are packaged in blisters of 28.
Marketing Authorization Holder and Manufacturer
Laboratorios Normon, S.A.
Ronda de Valdecarrizo, 6
28760 – Tres Cantos
Madrid (Spain)
Date of the Last Revision of this Leaflet: February 2023
Detailed information about this medicine is available on the website of the Spanish Agency for Medicines and Healthcare Products (AEMPS) http://www.aemps.gob.es/.
The average price of QUINAPRIL NORMON 40 mg FILM-COATED TABLETS in November, 2025 is around 9.3 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.
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