amlodipine and valsartan
Wamlox contains two active substances: amlodipine and valsartan. Both substances help control high blood pressure.
This means that both substances prevent blood vessels from constricting. As a result, blood vessels relax, and blood pressure decreases. Wamlox is used to treat high blood pressure in adult patients who are not adequately controlled with amlodipine or valsartan alone.
Before taking Wamlox, discuss with your doctor:
Your doctor may recommend regular monitoring of kidney function, blood pressure, and electrolyte levels (e.g., potassium) in the blood. See also "When not to take Wamlox".
If you experience stomach pain, nausea, vomiting, or diarrhea after taking Wamlox, discuss it with your doctor. Your doctor will decide on further treatment. Do not stop taking Wamlox on your own.
Wamlox should not be used in children and adolescents (under 18 years of age).
Tell your doctor or pharmacist about all medicines you are taking, have recently taken, or plan to take. Your doctor may recommend changing the dose and/or taking other precautions. In some cases, it may be necessary to stop taking one of the medicines. This is especially true for the following medicines:
Patients taking Wamlox should not eat grapefruits or drink grapefruit juice, as both grapefruits and grapefruit juice can lead to increased levels of the active substance amlodipine in the blood, which may result in unpredictable intensification of the effect of Wamlox, leading to a decrease in blood pressure.
Pregnancy
Tell your doctor if you are pregnant or planning to become pregnant. Your doctor will usually recommend stopping Wamlox before planned pregnancy or as soon as pregnancy is detected and recommend another medicine instead of Wamlox. Wamlox should not be used during early pregnancy (in the first 3 months) and should not be used after the third month of pregnancy, as it may seriously harm the baby if used after 3 months of pregnancy.
Breastfeeding
It has been shown that small amounts of amlodipine pass into human milk. Tell your doctor if you are breastfeeding or plan to breastfeed. Wamlox should not be used during breastfeeding. Your doctor may recommend alternative treatment if you want to breastfeed, especially in the case of a newborn or premature baby.
Before taking any medicine, consult your doctor or pharmacist.
This medicine may cause dizziness, which may affect your ability to concentrate. Therefore, do not drive, operate machinery, or perform other activities that require attention until you know how the medicine affects you.
This medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means it is essentially "sodium-free".
Take this medicine always as directed by your doctor. If you are unsure, ask your doctor. This will help you get the best results from the treatment and reduce the risk of side effects.
The usual dose of Wamlox is one tablet per day.
Depending on your response to treatment, your doctor may recommend a higher or lower dose of Wamlox.
Do not take a higher dose than recommended.
When increasing the dose, your doctor will exercise caution.
If you have any further questions about taking this medicine, ask your doctor or pharmacist.
If you have taken too many Wamlox tablets or if someone else has taken them by mistake, consult your doctor immediately.
Even 24-48 hours after taking the medicine, shortness of breath due to excess fluid accumulation in the lungs (pulmonary edema) may occur.
If you forget to take a dose, take it as soon as possible. Take the next dose at the usual time. However, if it is almost time for the next dose, skip the missed dose. Do not take a double dose to make up for the missed dose.
Stopping Wamlox treatment may worsen your condition. Do not stop taking Wamlox unless your doctor tells you to.
If you have any further questions about taking this medicine, ask your doctor or pharmacist.
Like all medicines, Wamlox can cause side effects, although not everybody gets them.
Severe side effects have occurred in a few patients (may affect less than 1 in 1000 people).
Allergic reaction with symptoms such as rash, itching, swelling of the face, lips, or tongue, difficulty breathing, low blood pressure (feeling weak, "empty" head).
Common (may affect less than 1 in 10 people):Flu; nasal congestion, sore throat, and discomfort when swallowing; headache; swelling of the arms, hands, legs, ankles, or feet; fatigue; asthenia (weakness); flushing and feeling of warmth on the face and (or) neck.
Uncommon (may affect less than 1 in 100 people):Dizziness; nausea and stomach pain; dryness of the mucous membranes; drowsiness, tingling, or numbness of the hands or feet; vertigo of labyrinthine origin, rapid heartbeat, including palpitations; dizziness when standing up; cough; diarrhea; constipation; skin rash, redness of the skin; swelling of the joints, back pain; joint pain.
Rare (may affect less than 1 in 1,000 people):Feeling of anxiety; ringing in the ears (tinnitus); fainting; increased urine production or feeling of strong urge to urinate; inability to achieve or maintain an erection; feeling of heaviness; low blood pressure with symptoms such as dizziness, feeling of "emptiness" in the head; excessive sweating; skin rash all over the body; itching; muscle cramps.
Amlodipine
The following side effects have been reported. If any of these side effects bother you or last more than a week, consult your doctor.
Common (may affect less than 1 in 10 people):dizziness, drowsiness; palpitations (feeling of heartbeat); sudden flushing; swelling of the ankles (edema); stomach pain, nausea.
Uncommon (may affect less than 1 in 100 people):mood changes, anxiety, depression, insomnia, tremors, taste disturbances, fainting, loss of sensation; vision disturbances, worsening of vision, tinnitus; low blood pressure; sneezing/ runny nose due to nasal inflammation (rhinitis); indigestion, vomiting; hair loss, increased sweating, itching of the skin, skin discoloration; urinary disturbances, increased need to urinate at night, increased frequency of urination; erectile dysfunction, discomfort or enlargement of the breasts in men, pain, poor general condition, muscle pain, muscle cramps; weight gain or weight loss.
Rare (may affect less than 1 in 1,000 people):disorientation.
Very rare (may affect less than 1 in 10,000 people):decreased white blood cell count, decreased platelet count, which can lead to unusual bruising and bleeding; increased blood glucose levels (hyperglycemia); gum swelling, abdominal bloating (gastritis); liver function disorders, liver inflammation, jaundice, increased liver enzyme activity, as shown in some test results; increased muscle tension; vasculitis, often with skin rash, hypersensitivity to light.
Unknown (frequency cannot be estimated from available data):tremors, stiffness, mask-like face, slow movements, and shuffling gait.
Valsartan
Very rare (may affect less than 1 in 10,000 people):Angioedema of the intestine: swelling in the intestine with symptoms such as stomach pain, nausea, vomiting, and diarrhea.
Unknown (frequency cannot be estimated from available data):decreased red blood cell count, fever, sore throat, or mouth ulcers due to infection; spontaneous bleeding or bruising; high potassium levels in the blood; abnormal liver function test results; kidney function disorders and kidney failure; swelling, mainly of the face and throat; muscle pain; rash, purple spots; fever; itching; allergic reactions, blistering of the skin (pemphigus).
If you experience any of these symptoms, tell your doctor immediately.
If you experience any side effects, including those not listed in this leaflet, tell your doctor or pharmacist. Side effects can be reported directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products Al. Jerozolimskie 181C, 02-222 Warsaw Tel.: +48 22 49 21 301 Fax: +48 22 49 21 309 Website: https://smz.ezdrowie.gov.pl Side effects can also be reported to the marketing authorization holder. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep the medicine out of sight and reach of children.
Do not use this medicine after the expiry date stated on the carton and blister. The expiry date refers to the last day of the month.
Store in a temperature below 30°C.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Wamlox, 5 mg + 80 mg, film-coated tablets Dark yellow, round, slightly biconvex film-coated tablets with beveled edges, with possible darker spots (tablet diameter: 8 mm, thickness: 3.0 mm - 4.3 mm).
Wamlox, 5 mg + 160 mg, film-coated tablets Dark yellow, oval, biconvex film-coated tablets, with possible darker spots (tablet dimensions: 13 mm x 8 mm, thickness: 3.8 mm - 5.4 mm).
Wamlox, 10 mg + 160 mg, film-coated tablets Light dark yellow, oval, biconvex film-coated tablets (tablet dimensions: 13 mm x 8 mm, thickness: 3.8 mm - 5.4 mm).
Cartons containing 10, 14, 28, 30, 56, 60, 84, 90, 98, and 100 film-coated tablets in OPA/Aluminum/PVC/Aluminum blisters.
Not all pack sizes may be marketed.
KRKA, d.d., Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia
KRKA, d.d., Novo mesto, Šmarješka cesta 6, 8501 Novo mesto, Slovenia TAD Pharma GmbH, Heinz-Lohmann-Straße 5, 27472 Cuxhaven, Germany KRKA - FARMA d.o.o., V.Holjevca 20/E, 10450 Jastrebarsko, Croatia
Date of last revision of the leaflet:19.03.2025
Austria, Croatia, Czech Republic, Estonia, Lithuania, Latvia, Poland, Romania, Slovakia, Slovenia, Hungary | Wamlox |
Bulgaria | Вамлокс |
Germany | Amlo-Valsacor |
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