Valsartan+Hydrochlorothiazide
Keep this leaflet, so you can read it again if you need to.
In case of any doubts, consult a doctor or pharmacist.
This medicine has been prescribed specifically for you. Do not pass it on to others.
The medicine may harm another person, even if their symptoms are the same.
If the patient experiences any side effects, including any not listed in this leaflet, they should tell their doctor or pharmacist. See section 4.
Co-Dipper film-coated tablets contain two active substances: valsartan and hydrochlorothiazide. Both
substances help control high blood pressure (hypertension).
Valsartanbelongs to a group of medicines called angiotensin II receptor antagonists, which help
control high blood pressure. Angiotensin II is a substance that narrows blood vessels in the body and
increases blood pressure. Valsartan blocks the action of angiotensin II, resulting in decreased blood vessel
tension and lower blood pressure.
Hydrochlorothiazidebelongs to a group of thiazide diuretics. Hydrochlorothiazide increases the amount of
urine excreted, which also lowers blood pressure.
Co-Dipper is used to treat high blood pressure that cannot be adequately controlled by either of the above
substances when used alone.
High blood pressure puts a strain on the heart and blood vessels. If left untreated, it can lead to damage to
blood vessels in the brain, heart, and kidneys, resulting in stroke, heart failure, or kidney failure. High blood
pressure increases the risk of heart attack. Lowering blood pressure to normal values reduces the risk of
these diseases.
if the patient is allergic to valsartan, hydrochlorothiazide, sulfonamide derivatives (substances with a
chemical structure similar to hydrochlorothiazide) or any of the other ingredients of this medicine (listed
in section 6);
if the patient is pregnant for more than 3 months (it is also recommended not to take Co-Dipper in early
pregnancy - see the section on pregnancy);
if the patient has severe liver disease, damage to the small bile ducts in the liver (cirrhosis), leading to
bile stagnation;
if the patient has severe kidney disease;
if the patient's body does not produce urine (anuria);
if the patient is undergoing dialysis ("artificial kidney");
if, despite treatment, the patient's blood potassium or sodium levels are lower than normal or if the blood
calcium level is higher than normal;
if the patient has gout;
if the patient has diabetes or kidney function disorders and is taking a blood pressure-lowering medicine
containing aliskiren.
the patient is taking potassium-sparing medicines, potassium supplements, salt substitutes containing
potassium, or other medicines that increase the amount of potassium in the blood (such as heparin),
regular monitoring of blood potassium levels by the doctor may be necessary.
the patient has low potassium levels in the blood.
the patient has diarrhea or severe vomiting.
the patient is taking high doses of diuretics.
the patient has severe heart disease.
the patient has heart failure or has had a heart attack; they should strictly follow the dose recommended
by the doctor. The doctor may also monitor the patient's kidney function.
the patient has narrowing of the renal artery.
the patient has recently received a new kidney (has undergone a kidney transplant).
the patient has been diagnosed with hyperaldosteronism - a disease in which the adrenal glands produce
too much aldosterone hormone; in such cases, the use of valsartan with hydrochlorothiazide is not
recommended.
the patient has liver or kidney disease.
the patient has previously experienced breathing or lung problems (including pneumonia or fluid buildup
in the lungs) after taking hydrochlorothiazide. If the patient experiences severe shortness of breath or
difficulty breathing after taking Co-Dipper, they should seek medical help immediately.
the patient is taking any of the following blood pressure-lowering medicines:
the doctor may recommend regular monitoring of kidney function, blood pressure, and electrolyte levels
(e.g., potassium) in the blood.
See also the information in the section "When not to take Co-Dipper".
The medicine may increase the sensitivity of the skin to sunlight.
If the patient is pregnant (or may become pregnant), they should inform their doctor.
Taking Co-Dipper is not recommended in early pregnancy and is contraindicated after the third month of
pregnancy, as its use at this time may be very harmful to the fetus (see the section "Pregnancy and
breastfeeding").
If the patient experiences stomach pain, nausea, vomiting, or diarrhea after taking Co-Dipper, they should
discuss it with their doctor. The doctor will decide on further treatment. The patient should not stop taking
Co-Dipper on their own.
Co-Dipper is not recommended for children and adolescents (under 18 years of age).
The effectiveness of the treatment may be affected by taking Co-Dipper and certain other medicines. It may be
necessary to change the dose and/or take other precautions, and in some cases, stop taking one of the
medicines.
This applies especially to the following medicines:
lithium, a medicine used to treat certain mental illnesses
medicines or substances that can increase the amount of potassium in the blood. These include potassium
supplements or salt substitutes containing potassium, potassium-sparing medicines, and heparin
medicines that can decrease the amount of potassium in the blood, such as diuretics, corticosteroids, laxatives,
carbenoxolone, amphotericin, or penicillin G
certain antibiotics (from the rifamycin group), a medicine to prevent transplant rejection (cyclosporine), or
a antiretroviral medicine used to treat HIV infection and AIDS (ritonavir). These medicines may enhance the
effect of Co-Dipper
medicines that can cause heart rhythm disturbances of the "torsades de pointes" type, such as anti-arrhythmic
medicines (used to treat heart rhythm disorders) and certain antipsychotic medicines
medicines that can decrease the amount of sodium in the blood, such as antidepressants, antipsychotics,
antiepileptics
medicines used to treat gout (such as allopurinol, probenecid, sulfinpyrazone)
therapeutically used vitamin D and calcium supplements
medicines used to treat diabetes (oral, e.g., metformin, or insulin)
other blood pressure-lowering medicines, including methyldopa, ACE inhibitors (e.g., enalapril, lisinopril, etc.)
or aliskiren (see also the information in the section "When not to take Co-Dipper" and "Warnings and
precautions")
medicines used to increase blood pressure, such as noradrenaline or adrenaline
digoxin or other digitalis glycosides (medicines used to treat heart rhythm disorders)
medicines that can increase blood sugar levels, such as diazoxide or beta-adrenolytics
cytotoxic medicines (used to treat cancer), such as methotrexate or cyclophosphamide
painkillers, such as nonsteroidal anti-inflammatory drugs (NSAIDs), including selective cyclooxygenase-2
(COX-2) inhibitors and acetylsalicylic acid in doses greater than 3 grams per day
muscle relaxants, such as tubocurarine
anticholinergic medicines (used to treat various diseases, such as stomach and intestinal cramps, urinary
bladder cramps, asthma, motion sickness, muscle cramps, Parkinson's disease, and as part of general
anesthesia)
amantadine (a medicine used to treat Parkinson's disease and to treat and prevent certain viral infections)
cholestyramine and colestipol (medicines used mainly to treat high fat levels in the blood)
cyclosporine (a medicine used to prevent transplant rejection)
alcohol, sleeping pills, and anesthetics (medicines with a sedative or analgesic effect, used, for example,
during surgery)
iodinated contrast agents (used in imaging studies).
Co-Dipper can be taken with or without food.
The patient should not consume alcohol without first consulting their doctor. Alcohol may enhance the
lowering of blood pressure and/or cause dizziness or fainting.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a baby, they should
consult their doctor or pharmacist before taking this medicine.
The patient must inform their doctor if they are pregnant (or may become pregnant).
The doctor will recommend stopping Co-Dipper before the patient becomes pregnant or as soon as possible
after pregnancy is confirmed, and will offer an alternative medicine. Co-Dipper is not recommended in early
pregnancy; it must not be taken after the third month of pregnancy, as it may seriously harm the fetus.
The patient must inform their doctor if they are breastfeeding or plan to breastfeed.
Taking Co-Dipper is not recommended during breastfeeding. For patients planning to breastfeed, especially
newborns or premature babies, the doctor may choose a different, more suitable medicine.
Before driving, using tools, operating machinery, or performing tasks that require concentration, the patient
should make sure how Co-Dipper affects their body. Like other medicines used to treat high blood pressure,
Co-Dipper can rarely cause dizziness, which can affect concentration.
To get the best results from the treatment and minimize the risk of side effects, this medicine should always be
taken as directed by the doctor. If the patient has any doubts, they should consult their doctor or pharmacist.
People with high blood pressure often do not feel any symptoms of their illness. Many of them feel perfectly well.
Therefore, it is very important to attend doctor's appointments, even if the patient feels well.
The doctor will determine the exact number of Co-Dipper tablets the patient should take. The doctor may
recommend taking a higher or lower dose of the medicine, depending on the patient's response to the
treatment.
The usual recommended dose of Co-Dipper is one tablet per day.
The patient should not change the dose of the medicine or stop taking the tablets without consulting their
doctor.
The medicine should be taken at the same time every day, usually in the morning.
Co-Dipper can be taken with or without food.
The tablets should be swallowed with a glass of water.
If the patient experiences severe dizziness and/or fainting, they should lie down and contact their doctor
immediately.
If the patient accidentally takes too many tablets, they should contact their doctor, pharmacist, or hospital.
If the patient misses a dose, they should take it as soon as possible after remembering.
If it is almost time for the next dose, they should skip the missed dose.
The patient should not take a double dose to make up for the missed dose.
Stopping Co-Dipper treatment may cause a worsening of high blood pressure. The patient should not stop taking
the medicine without their doctor's advice.
Like all medicines, Co-Dipper can cause side effects, although not everybody gets them.
The patient should contact their doctor immediately if they experience symptoms of angioedema, such as:
swelling of the face, tongue, or throat
difficulty swallowing
hives and difficulty breathing.
The patient should also contact their doctor immediately if they experience acute respiratory failure (symptoms
include severe shortness of breath, fever, weakness, and confusion). This side effect is very rare (may occur
less often than in 1 in 10,000 patients).
Uncommon (affect 1 to 10 users in 1000)
cough
low blood pressure
dizziness
dehydration (with increased thirst, dry mouth and tongue, infrequent urination, dark urine, dry skin)
muscle pain
fatigue
tingling or numbness
blurred vision
ringing in the ears (e.g., hissing, buzzing)
Rare (affect 1 to 10 users in 10,000)
dizziness
diarrhea
joint pain
Frequency not known (cannot be estimated from the available data)
breathing difficulties
significantly reduced urine output
low sodium levels in the blood (which can cause fatigue, confusion, muscle twitching, and/or seizures in
severe cases)
low potassium levels in the blood (sometimes with muscle weakness, muscle cramps, irregular heartbeat)
low white blood cell count (with symptoms such as fever, skin or throat infections, mouth ulcers due to
infection, weakness)
increased bilirubin levels in the blood (which can cause yellowing of the skin and eyes in severe cases)
increased urea and creatinine levels in the blood (which may indicate kidney function disorders)
increased uric acid levels in the blood (which can cause gout in severe cases)
fainting
Valsartan
Uncommon (affect 1 to 10 users in 1000)
vertigo
abdominal pain
Rare (affect less than 1 user in 10,000)
angioedema of the intestine: intestinal swelling with symptoms such as abdominal pain, nausea, vomiting,
and diarrhea
Frequency not known (cannot be estimated from the available data)
blistering of the skin (a symptom of bullous dermatitis)
skin rash with itching or without itching, along with some of the following symptoms: fever, joint pain,
muscle pain, swollen lymph nodes, and/or flu-like symptoms
skin rash, purpura, fever, itching (symptoms of vasculitis)
low platelet count (sometimes with bleeding or bruising)
high potassium levels in the blood (sometimes with muscle cramps, irregular heartbeat)
allergic reactions (with symptoms such as rash, itching, hives, difficulty breathing or swallowing, dizziness)
swelling, mainly of the face and throat; rash; itching
increased liver enzyme activity
decreased hemoglobin and red blood cell count (which can cause anemia in severe cases)
kidney failure
low sodium levels in the blood (which can cause fatigue, confusion, muscle twitching, and/or seizures in
severe cases)
Hydrochlorothiazide
Very common (affect more than 1 user in 10)
low potassium levels in the blood
increased fat levels in the blood
Common (affect 1 to 10 users in 100)
low sodium levels in the blood
low magnesium levels in the blood
high uric acid levels in the blood
itching rash and other types of rash
decreased appetite
mild nausea and vomiting
dizziness, fainting when standing up
erectile dysfunction
Rare (affect 1 to 10 users in 10,000)
swelling and blistering of the skin (due to increased sensitivity to sunlight)
high calcium levels in the blood
high blood sugar levels
presence of sugar in the urine
worsening of diabetic metabolic disorders
constipation, diarrhea, discomfort in the stomach or intestines, liver function disorders (which may be
accompanied by yellowing of the skin and eyes)
irregular heartbeat
headache
sleep disturbances
depression
low platelet count (sometimes with bleeding or bruising)
dizziness
tingling or numbness
vision disturbances
Very rare (affect less than 1 user in 10,000)
vasculitis with symptoms such as rash, purpura, fever
skin rash, itching, hives, difficulty breathing or swallowing, dizziness (allergic reactions)
severe skin disease causing rash, redness of the skin, blistering around the lips, eyes, or mouth, skin
peeling, fever (toxic epidermal necrolysis)
rash on the face, joint pain, muscle disorders, fever (lupus erythematosus)
severe abdominal pain (pancreatitis)
breathing difficulties with fever, cough, wheezing, shortness of breath (respiratory failure, including
pneumonia and pulmonary edema)
fever, sore throat, frequent infections (agranulocytosis)
pale skin, fatigue, shortness of breath, dark urine (hemolytic anemia)
fever, sore throat, or mouth ulcers due to infection (leukopenia)
confusion, fatigue, twitching, and muscle cramps, rapid breathing (hypochloremic alkalosis)
Frequency not known (cannot be estimated from the available data)
weakness, bruising, and frequent infections (aplastic anemia)
significantly reduced urine output (possible sign of kidney function disorders or kidney failure)
vision loss or eye pain due to increased pressure in the eyeball (possible symptoms of fluid accumulation in
the vascular layer of the eye - excessive fluid accumulation between the choroid and sclera - or acute angle-
closure glaucoma)
skin rash, redness of the skin, blistering around the lips, eyes, or mouth, skin peeling, fever (possible
symptoms of erythema multiforme)
muscle cramps
fever
weakness
skin cancers and lip cancers (non-melanoma skin cancers)
If the patient experiences any side effects, including any not listed in this leaflet, they should tell their doctor,
pharmacist, or nurse. 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.
Reporting side effects will help to gather more information on the safety of this medicine.
The medicine should be stored out of sight and reach of children.
Do not use this medicine after the expiry date stated on the blister pack and carton after EXP. The expiry date
refers to the last day of that month.
Do not store above 30°C.
Store in the original package to protect from moisture.
Do not use Co-Dipper if the packaging is damaged or shows signs of tampering.
Medicines should not be disposed of via wastewater or household waste. The patient should ask their
pharmacist how to dispose of medicines they no longer use. This will help protect the environment.
The active substances are valsartan and hydrochlorothiazide.
Each tablet contains 80 mg of valsartan and 12.5 mg of hydrochlorothiazide.
The other ingredients are: microcrystalline cellulose, crospovidone, magnesium stearate, colloidal anhydrous
silica.
Coating:hypromellose, macrogol 8000, talc, titanium dioxide (E171), iron oxide red (E172), iron oxide
yellow (E172).
Light orange, oval, slightly convex film-coated tablet with a symbol "HGH" embossed on one side and "CG"
on the other side.
Pack sizes: 14, 28, 30, 56, 60, or 98 film-coated tablets.
Marketing authorization holder
Sandoz GmbH
Biochemiestrasse 10
6250 Kundl, Austria
Manufacturer/Importer
Lek Pharmaceuticals d.d.
Verovškova 57
1526 Ljubljana, Slovenia
Lek Pharmaceuticals d.d.
Trimlini 2D
9220 Lendava, Slovenia
Lek S.A.
ul. Domaniewska 50 C
02-672 Warsaw
Lek S.A.
ul. Podlipie 16
95-010 Stryków
Novartis Farma S.p.A
Via Provinciale Schito 131
I-800058 Torre Annunziata / NA
Italy
Salutas Pharma GmbH
Otto-von-Guericke-Allee 1
39179 Barleben, Germany
Sandoz, S.R.L.
Livezeni Street no 7A
540472 Targu Mures, Romania
Sandoz Polska Sp. z o.o.
ul. Domaniewska 50 C
02-672 Warsaw
tel. 22 209 70 00
Date of last revision of the leaflet:01/2025
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