Wytens Side Effects

Common Wytens Side Effects

The most commonly reported Wytens side effects (click to view or check a box to report):

Blood Lactate Dehydrogenase Increased (2)
Systemic Lupus Erythematosus (2)
Loss Of Consciousness (2)
Blood Triglycerides Increased (2)
Cerebrovascular Accident (2)
Renal Failure Acute (1)
Proteinuria (1)
Eczema (1)
Anaemia Haemolytic Autoimmune (1)
Oedema Peripheral (1)
Amnesia (1)
Double Stranded Dna Antibody (1)
Malaise (1)
Hyperproteinaemia (1)
International Normalised Ratio Increased (1)
Glycosylated Haemoglobin Increased (1)
Fatigue (1)
Nephrotic Syndrome (1)
Memory Impairment (1)
Oedema Genital (1)

➢ More

If you or someone in your family has experienced a serious side effect to a health product, you are encouraged to report the experience to your health care professional (e.g. physician, pharmacist). You could also complete a copy of the side effect reporting form or report your side effect to FDA.

Side effects reports are analyzed to discover potential health product safety signals. Some important reactions may take an extremely long time to develop or occur infrequently. Continued monitoring of adverse reactions is thus essential to maintain a comprehensive safety and effectiveness profile of health products.

Wytens Side Effects Reported to FDA

The following Wytens reports list potential signals of serious risks and new safety information that were identified using the FDA Adverse Event Reporting System (FAERS).
FAERS is a database that contains information on adverse event and medication errors reports submitted to FDA by healthcare professionals (such as physicians, pharmacists, nurses and others), consumers (such as patients, family members, layers and others) and manufacturers.

The appearance of Wytens on this list does not mean that FDA has concluded that the drug has the listed risk. It means that FDA has identified a potential safety issue, but it does not mean that FDA has found a causal relationship between the drug and the listed risk.
International Normalised Ratio Increased
This is a report of a male patient (weight: NA) from JAPAN, suffering from the following symptoms/conditions: hypertension,atrial fibrillation, who was treated with Wytens (dosage: 2 Mg, start time: Jul 14, 2011), combined with:
  • Pradaxa (220 Mg)
  • Amlodipine (5 Mg)
  • Diovan (80 Mg)
  • Doxazon (2 Mg)
  • Kallikrein (30 Mg)
and developed a serious reaction and side effect(s). The consumer presented with:
  • International Normalised Ratio Increased
which developed after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Wytens treatment in male patients, resulting in international normalised ratio increased side effect.

Oedema Genital, Nephrotic Syndrome, Oedema Peripheral
This report suggests a potential Wytens Oedema Genital, Nephrotic Syndrome, Oedema Peripheral side effect(s) that can have serious consequences. A 68-year-old male patient (weight: NA) from JAPAN was diagnosed with the following symptoms/conditions: NA and used Wytens (dosage: NA) starting Jan 01, 2008. Soon after starting Wytens the patient began experiencing various side effects, including:
  • Oedema Genital
  • Nephrotic Syndrome
  • Oedema Peripheral
Drugs used concurrently:
  • Corinael
  • Pamilcon
  • Lipitor
  • Lantus
  • Cilostazol
  • Diovan
Although Wytens demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as oedema genital, may still occur.

Anaemia Haemolytic Autoimmune, Antiphospholipid Syndrome, Coombs Positive Haemolytic Anaemia, Cytolytic Hepatitis, Double Stranded Dna Antibody, Hyperproteinaemia, Systemic Lupus Erythematosus
This Anaemia Haemolytic Autoimmune, Antiphospholipid Syndrome, Coombs Positive Haemolytic Anaemia, Cytolytic Hepatitis, Double Stranded Dna Antibody, Hyperproteinaemia, Systemic Lupus Erythematosus problem was reported by a consumer or non-health professional from FRANCE. A 71-year-old female patient (weight: NA) was diagnosed with the following symptoms/conditions: hypertension. On Dec 11, 2006 this consumer started treatment with Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate) (dosage: Oral). The following drugs were being taken at the same time:
  • Rabeprazole Sodium (Oral)
  • Xanax (0,125 Mg (0,1125 Mg, 1 In 1 D) Oral)
When commencing Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate), the patient experienced the following unwanted symptoms/side effects:
  • Anaemia Haemolytic Autoimmune
  • Antiphospholipid Syndrome
  • Coombs Positive Haemolytic Anaemia
  • Cytolytic Hepatitis
  • Double Stranded Dna Antibody
  • Hyperproteinaemia
  • Systemic Lupus Erythematosus
The patient was hospitalized.Although all drugs are carefully tested before they are licensed for use, they carry side effect risks. Some side effects, such as anaemia haemolytic autoimmune, may become evident only after a product is in use by the general population.

Condition Aggravated, Diabetes Mellitus, Fatigue, Systemic Lupus Erythematosus
This is a report of a 65-year-old female patient (weight: NA) from FRANCE. The patient developed the following symptoms/conditions: hypertension and was treated with Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate) (dosage: Oral) starting Jan 01, 2004. Concurrently used drugs: NA.Soon after that, the consumer experienced the following side effects:
  • Condition Aggravated
  • Diabetes Mellitus
  • Fatigue
  • Systemic Lupus Erythematosus
This opens a possibility that Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate) treatment could cause the above reactions, including condition aggravated, and some female subjects may be more susceptible.

Amnesia, Delirium, Memory Impairment, Road Traffic Accident
A 56-year-old male patient (weight: NA) from JAPAN with the following symptoms/conditions: NA started Wytens treatment (dosage: 2 Mg) on Aug 02, 2003. Soon after starting Wytens treatment, the subject experienced various side effects, including:
  • Amnesia
  • Delirium
  • Memory Impairment
  • Road Traffic Accident
Concurrently used drugs:
  • Diovan (80 Mg)
  • Myslee (10 Mg)
This finding indicates that some male patients could be more vulnerable to Wytens.

A 75-year-old male patient from FRANCE (weight: NA) experienced symptoms, such as: NA and was treated with Wytens /spa/(dosage: NA). The treatment was initiated on NS. After that a consumer reported the following side effect(s):
  • Eczema
Concurrently used drugs, which potentially could have contributed to side effect(s) or affected Wytens /spa/ efficacy:
  • Befizal
  • Allopurinol
  • Xanax
  • Tareg (160 Mg, Qd)

Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Carotid Artery Atheroma, Cerebrovascular Accident, Loss Of Consciousness, Renal Failure Acute
In this report, Wytens (bisoprolol/hydrochlorothiazide, Tablet, 0) was administered for the following condition: NA.A 58-year-old male consumer from (weight: NA) started Wytens (bisoprolol/hydrochlorothiazide, Tablet, 0) treatment (dosage: See Image) on NS.Sometime after starting the treatment, the patient complained of the following side effect(s):
  • Blood Lactate Dehydrogenase Increased
  • Blood Triglycerides Increased
  • Carotid Artery Atheroma
  • Cerebrovascular Accident
  • Loss Of Consciousness
  • Renal Failure Acute
A possible interaction with other drugs could have contributed to this reaction:
  • Valsartan (160 Mg 1x Per 1 Day Oral)
  • Daonin (glibenclamide)
  • Di-actane (naftidrofuryl Oxalate)
  • Allopurinol
  • Plavix
The patient was hospitalized.Establishing a causal relationship between a specific drug and consumer's side effects is complex, but it is possible that in this report Wytens (bisoprolol/hydrochlorothiazide, Tablet, 0) treatment could be related to the listed above side effect(s).

Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Blood Urea Increased, Cerebrovascular Accident, Glycosylated Haemoglobin Increased, Loss Of Consciousness, Malaise, Proteinuria
This is a report of the following Wytens side effect(s):
  • Blood Creatinine Increased
  • Blood Lactate Dehydrogenase Increased
  • Blood Triglycerides Increased
  • Blood Urea Increased
  • Cerebrovascular Accident
  • Glycosylated Haemoglobin Increased
  • Loss Of Consciousness
  • Malaise
  • Proteinuria
A 58-year-old male patient from (weight: NA) presented with the following condition: NA and received a treatment with Wytens (dosage: 10 Mg, Qd) starting: NS.The following concurrently used drugs could have generated interactions:
  • Daonil
  • Di-actane (200 Mg, Bid)
  • Allopurinol (200 Mg, Qd)
  • Tareg (160 Mg, Qd)
  • Plavix (75 Mg, Qd)
The patient was hospitalized.This report suggests that a Wytens treatment could be associated with the listed above side effect(s).

Keep Track of Side Effects

Note Your Observations

It is really important to keep of your symptoms, right from the time you start a new medicine. You can do it any way you prefer: in a notebook, in a computer file or using our online tool. You should also note down any other medicines you are taking at the same time, because there could be an interaction between these medicines.

Why Your Notes are Important

Your notes could be helpful in several ways:

  • You can use them to remind you of details that may alert your health care professional(s) to a problem
  • You will have a record to refer to in the future, in case you are ever prescribed the same medicine again

  • Log Form

    You can use the following log form to write down important information, like the date and time you experienced a side effect and your symptoms, how strong the symptoms were, and any other medicines you were using.

    Medicine Name and Dosage:
    Side Effects Scale Date & Time Other Medicine(s) or Treatment(s)
    Scale: 1 = very mild to 10 = very bad

    You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

    Discuss Wytens Side Effects

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    Wytens Safety Alerts, Active Ingredients, Usage Information

    More About Wytens

    Side Effects reported to FDA: 8

    Wytens safety alerts: No

    Reported hospitalizations: 1

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