Zuandol 100 mg Film-Coated Tablets
Sildenafil Citrate
Read this leaflet carefully before you start taking this medicinebecause it contains important information for you
Zuandol contains the active ingredient sildenafilo, which belongs to a group of medicines called phosphodiesterase type 5 (PDE5) inhibitors. It works by dilating the blood vessels of the penis, allowing blood to flow when sexually stimulated. Zuandol will only help achieve an erection if you are sexually stimulated.
Zuandol is indicated for the treatment of male erectile dysfunction, sometimes referred to as impotence. This occurs when a man is unable to obtain or maintain a firm, adequate erection for satisfactory sexual activity.
Warnings and precautions
Consult your doctor, pharmacist, or nurse before starting to take Zuandol:
Zuandol is not recommended to be used simultaneously with any other oral or local treatment for erectile dysfunction.
Do not take Zuandol with treatments for pulmonary arterial hypertension (PAH) that contain sildenafil or any other PDE5 inhibitor.
Do not take Zuandol if you do not have erectile dysfunction.
The use of Zuandol is not indicated in women.
Children and adolescents
The use of Zuandol is not indicated in individuals under 18 years of age.
Special considerations in patients with renal or hepatic problems
You must inform your doctor if you have renal or hepatic problems. Your doctor may decide to reduce your dose.
Other medications and Zuandol
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
Zuandol tablets may interact with some medications, especially those used to treat chest pain. In case of a medical emergency, you must inform your doctor, pharmacist, or nurse that you are taking Zuandol and when you took it. Do not take Zuandol with other medications unless your doctor advises you to.
Do not take Zuandol if you are taking medications called nitrates, as the combination may cause a dangerous drop in your blood pressure. Always inform your doctor, pharmacist, or nurse if you are taking any of these medications, which are often used to relieve chest pain (or "chest pain").
Do not take Zuandol if you are taking medications called nitric oxide donors, such as amyl nitrite ("poppers"), as the combination may cause a dangerous drop in your blood pressure.
Inform your doctor or pharmacist if you are taking riociguat.
If you are taking medications known as protease inhibitors, such as those used to treat HIV, your doctor may recommend that you start treatment with the lowest dose (25 mg) of sildenafil.
Some patients taking an alpha-blocker, a medication used to treat high blood pressure or prostate enlargement, may experience dizziness or lightheadedness that may be caused by a drop in blood pressure when sitting or standing up quickly. Some patients have experienced these symptoms when taking Zuandol with alpha-blockers. This is more likely to occur in the 4 hours following Zuandol intake. To reduce the likelihood of these symptoms, you should be receiving your daily dose of the alpha-blocker regularly before starting Zuandol. Your doctor may recommend that you start treatment with the lower dose (25 mg) of sildenafil.
Inform your doctor or pharmacist if you are taking medications that contain sacubitril/valsartan, used to treat heart failure.
Use of Zuandol with food, drinks, and alcohol
Zuandol can be taken with or without food. However, you may notice that Zuandol takes a bit longer to take effect if taken with a large meal.
Consuming alcohol may temporarily impair your ability to achieve an erection. Therefore, to get the maximum benefit from the medication, it is recommended not to consume large amounts of alcohol before taking Zuandol.
Pregnancy, breastfeeding, and fertility
The use of Zuandol is not indicated in women.
Driving and operating machinery
Zuandol may cause dizziness and affect your vision. You must know how you react to Zuandol before driving vehicles or operating machinery.
Zuandol contains sodium
Follow exactly the administration instructions for this medication as indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.
The recommended starting dose is 50 mg.
Do not takeZuandol more than once a day.
Do not take Zuandol film-coated tablets withother medications that contain sildenafil.
Take Zuandol approximately one hour before planning to have sexual intercourse. Swallow the tablet whole with a glass of water.
If you notice that the effect of this medication is too strong or too weak, inform your doctor or pharmacist.
Zuandol will only help you achieve an erection if you are sexually stimulated. The time it takes to take effect varies from person to person, generally ranging from 30 minutes to one hour. The effect of this medication may be delayed if taken with a large meal.
If Zuandol does not help you achieve an erection or if the erection does not last long enough to complete sexual intercourse, consult your doctor.
If you take more Zuandol than you should
You may experience an increase in adverse effects and their severity. Doses above 100 mg do not increase efficacy.
Do not take more tablets than recommended by your doctor.
In case of overdose or accidental ingestion, consult your doctor or pharmacist, or call the Toxicological Information Service, phone 915 620 420 (indicating the medication and the amount ingested).
Contact your doctor if you have taken more tablets than advised. You can also consult immediately with your pharmacist or call the Toxicological Information Service, phone 915 620 420, indicating the medication and the amount ingested.
If you have any doubts about the use of this medication, ask your doctor, pharmacist, or nurse.
If you experience any of the following serious side effects, stop taking Zuandol and seek medical attention immediately:
If they occur during or after sexual intercourse:
Other side effects:
Very common(may affect more than 1 in 10 people): headache.
Common(may affect up to 1 in 10 people): nausea, facial flushing, warmth (including symptoms such as sudden heat sensation in the upper body), indigestion, abnormal color perception, blurred vision, visual deterioration, nasal congestion, and dizziness.
Uncommon(may affect up to 1 in 100 people): vomiting, skin eruptions,eye irritation, eye discharge/ red eyes, eye pain,lightning-like vision, visual clarity, light sensitivity, watery eyes,palpitations, rapid heart rate,high blood pressure, low blood pressure,muscle pain, feeling of drowsiness, reduced tactile sensation, vertigo, ringing in the ears,dry mouth,nasal congestion or blockage, nasal mucosa inflammation (including symptoms such as coughing, sneezing, and nasal congestion), upper abdominal pain, gastroesophageal reflux disease (including symptoms such as stomach burning), blood in urine,arm or leg pain,nosebleed,sensation of heat and feeling of fatigue.
Rare(may affect up to 1 in 1000 people): fainting, stroke, heart attack, irregular heartbeat, transient decrease in blood flow to some parts of the brain, sensation of throat constriction, numbness of the mouth, bleeding in the back of the eye, double vision, visual acuity decrease, abnormal sensation in the eye, eye swelling or eyelid swelling, small particles or spots in vision, halos around lights, pupil dilation, change in color of the white part of the eye, bleeding of the penis, blood in semen, dry nose, nasal interior swelling, sensation of irritability, and sudden decrease or loss of hearing.
During post-marketing experience, rare cases of unstable angina (heart disease) and sudden death have been reported. It is worth noting that most men who experienced these side effects, although not all of them, had heart problems before taking this medicine. It is not possible to determine if these side effects were directly related to Zuandol.
Reporting side effects:
If you experience any type of side effect, consult your doctor or pharmacist, even if it is a possible side effect that does not appear 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.
Keepthis medicationout of the sight and reach of children.
Store in the original packaging to protect it from moisture.
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.
Medications should not be disposed of through drains ortrash. Dispose of the packaging and medications you no longer need at the SIGREcollection pointat the pharmacy.If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
Core tablet:microcrystalline cellulose, dibasic calcium phosphate, sodium croscarmellose, and magnesium stearate.
Coating:polyvinyl alcohol, polyethylene glycol 3350, titanium dioxide (E171), talc, and aluminum lake of indigo carmine.
Appearance of the product and contents of the package
Zuandol 100 mg tablets have a coating, are elliptical in shape, and are blue in color. They are engraved with “+” on one face.
Zuandol 100 mg is presented in blisters of 4 or 8 tablets per package.
Only some package sizes may be commercially available.
Other presentations:
Zuandol 50 mg, packages with 1, 2, 4, or 8 tablets.
Holder of the marketing authorization and responsible for manufacturing
Holder:
GP-Pharm, S.A.
Industrial Park Els Vinyets – Els Fogars, sector 2
Carretera Comarcal C244, Km 22,
08777 – Sant Quintí de Mediona (Barcelona) SPAIN
Tel: 93 6388000
Fax: 93 6389393
Responsible for manufacturing:
Atlantic Pharma - Producções Farmacêuticas, S.A.
Rua da Tapada Grande, nº2, Abrunheira, 2710-089 Sintra(Portugal)
Last review date of this leaflet:March2025
Detailed information about this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.es/.
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