Package Leaflet: Information for the User
Quinapril Normon 40 mg Film-Coated Tablets
Read this leaflet carefully before you start taking this medicine, because it contains important information for you.
Quinapril belongs to the angiotensin-converting enzyme inhibitors (ACE inhibitors). It works by dilating blood vessels. This makes it easier for the heart to pump blood to all parts of the body and helps to reduce high blood pressure.
Your doctor has prescribed quinapril for the treatment of:
-high blood pressure.
-congestive heart failure.
The treatment with Quinapril Normon requires periodic monitoring by your doctor.
Do not take Quinapril Normon
Warnings and precautions
Consult your doctor or pharmacist before starting to take Quinapril Normon:
Consult your doctor if you experience dizziness and vertigo. If dizziness appears, lie down until this sensation passes. After lying down, always get up slowly to avoid dizziness. If you faint or feel dizzy, inform your doctor.
As with other ACE inhibitors, taking Quinapril Normon may cause dry cough, which disappears when the treatment is stopped. In this case, consult your doctor.
Consult your doctor if any of the circumstances mentioned above have ever occurred to you.
Your doctor may monitor your kidney function, blood pressure, and electrolyte levels in the blood (for example, potassium), at regular intervals.
See also the information under the heading "Do not take Quinapril Normon."
Consult your doctor or pharmacist before taking a medication.
Patients over 65 years old
If you are elderly, you may be more sensitive to the effects mentioned above. If any of these effects appear, inform your doctor immediately.
Use of Quinapril Normon with other medications
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication, including those purchased without a prescription.
Your doctor may need to modify your dose and/or take other precautions:
If you are taking an angiotensin II receptor antagonist (ARA) or aliskirén (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 medication. Inform your doctor that you are receiving treatment with Quinapril Normon if you are to undergo any surgical procedure.
Quinapril Normon may interact with the following medications. It is especially important to inform your doctor if you are taking:
If you have any doubts about taking other medications with Quinapril Normon, consult your doctor.
Use of Quinapril Normon with food and drinks
Quinapril Normon can be taken with or without food.
Pregnancy, lactation, and fertility
If you are pregnant or breastfeeding, or think you may be pregnant or plan to become pregnant, consult your doctor before using this medication.
Pregnancy:
Inform your doctor if you think you are or may be pregnant. Normally, your doctor will instruct you to stop taking Quinapril Normon before becoming pregnant or as soon as you know you are pregnant and will instruct you to take another medication instead of Quinapril Normon. Quinapril Normon is not recommended at the beginning of pregnancy, and it should not be taken after the third month of pregnancy, as it may cause serious harm to your baby if used at that time.
Lactation
Consult your doctor or pharmacist before using a medication.
Inform your doctor if you are breastfeeding or about to start breastfeeding. Quinapril Normon is not recommended 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 medication during breastfeeding, compared to other treatments.
Driving and operating machines
Quinapril Normon may cause a sudden drop in blood pressure, causing dizziness and, in some cases, fainting. This may occur especially during the first days of treatment. Therefore, do not perform tasks that require special attention (for example, driving a car or operating hazardous machinery) until you know how you tolerate the treatment.
Follow exactly the administration instructions of this medication as indicated by your doctor. In case of doubt, consult your doctor again.
Remember to take your medication.
Your doctor will indicate the duration of your treatment with Quinapril Normon. Your doctor may increase or decrease the dose as needed until they find the dose you need. Do not stop treatment beforehand, as your blood pressure may rise or your heart function may worsen.
This treatment has been indicated by your doctor specifically for you and your disease. The dose will be established by the doctor based on the needs of each patient. Depending on the individual response, the doctor may modify the quinapril dosing. Follow your doctor's instructions faithfully regarding the dose and mode 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 medication
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). You can take them with meals or without them.
If you estimate that the action of this medication 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 Toxicological Information Service, Teléfono 91 562 04 20. Bring this leaflet with you.
The most probable symptom that could be expected after an overdose of quinapril would be a decrease in blood pressure. Symptomatic treatment will be performed to compensate for the effects of this medication.
In severe cases, the necessary measures will be taken; in addition to maintaining blood volume, it may be necessary to administer medications that restore your blood pressure adequately.
If you forgot to take Quinapril Normon
Do not take a double dose to compensate for the missed doses.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
If you interrupt treatment with Quinapril Normon
Your doctor will indicate the duration of your treatment with Quinapril Normon. Do not stop taking Quinapril Normon without consulting them. Normally, medications for treating high blood pressure or heart failure should be taken for life. If you stop taking Quinapril Normon, it may worsen.
If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
Like all medicines, this medicine may cause side effects, although not everyone will experience them.
Quinapril side effects vary in intensity from one individual to another, and should be taken into account especially at the beginning of treatment, when changing the dose or switching medications.
Stop taking Quinapril Normon and contact your doctor immediately if:
- Difficulty breathing with or without facial, lip, tongue, and/or throat inflammation occurs.
- Facial, lip, tongue, and/or throat inflammation occurs that may cause difficulty swallowing.
The following are possible side effects during treatment with Quinapril Normon, listed by frequency.
Side effectsfrequent(may affect between 1 to 10 people per 100)are: Headache, dizziness, nasal mucosa inflammation (rhinitis), cough, fatigue, weakness (asthenia), nausea and/or vomiting, muscle pain (myalgia), diarrhea, chest pain, abdominal pain, digestive discomfort (dyspepsia), difficulty breathing (dyspnea), back pain, pharyngeal inflammation (pharyngitis), difficulty falling asleep (insomnia), elevated levels of certain substances in blood tests (potassium, creatinine, and urea nitrogen), decreased sodium levels in the blood, low blood pressure (hypotension), and paresthesias.
Side effectsinfrequent (may affect between 1 to 10 people per 1,000)are: Palpitations, vasodilation, chest tightness (angina pectoris), increased heart rate (tachycardia), myocardial infarction, flatulence, dry mouth or throat, depression, nervousness, confusion, drowsiness, transient interruption of blood supply to a brain area (transient ischemic attack), vertigo, tinnitus, nasal sinus inflammation (sinusitis), upper respiratory tract infection, bronchitis, allergic reaction with facial, tongue, or throat swelling that may cause difficulty breathing (angioedema), urinary tract infections, kidney function impairment, proteinuria, impotence, decreased visual acuity (amblyopia), fever, and excessive fluid accumulation in the body (edema).
Side effectsrare (may affect up to 1 person per 1,000)are: Balance disorder, syncope, respiratory disease (eosinophilic pneumonia), taste alteration, constipation, tongue inflammation, urticaria, and various skin lesions that may be severe (erythema multiforme, pemphigus).
Side effectsvery rare (may affect up to 1 person per 10,000)are: Blurred vision, intestinal obstruction (ileus), intestinal inflammation (intestinal angioedema), and skin rash similar to psoriasis.
Reporting of 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 prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicines for Human Use: https://www.notificaram.es. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.
Store below 30°C.
Medications should not be disposed of through drains or in the trash. Dispose of packaging and medications you no longer need at the SIGRE point of your pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Quinapril Normon 40 mg film-coated tablets
-The active ingredient is quinapril. Each film-coated tablet contains 40 mg of quinapril.
-The other components are: magnesium carbonate, hydroxypropylcellulose, crospovidone, magnesium stearate, Eudragit E 12.5%, titanium dioxide (E-171), talc, macrogol 6000, and iron oxide yellow (E-172).
Appearance of the product and content of the packaging
Round, biconvex tablets of brown color.
The tablets are packaged in blisters of 28.
Holder of the marketing authorization and responsible for manufacturing
Normon Laboratories, S.A.
Ronda de Valdecarrizo, 6
28760 – Tres Cantos
Madrid (Spain)
Last review date of this leaflet: February 2023
The detailed information of this medication is available on the website of the Spanish Agency of Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es/.
Have questions about this medication or your symptoms? Connect with a licensed doctor for guidance and personalized care.