PatientsVille.com Logo

Wytens Side Effects

PatientsVille

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.

Wytens Side Effects Reported to FDA



Wytens Side Effect Report#7893482-4
International Normalised Ratio Increased
This is a report of a male patient (weight: NA) from Japan, suffering from the following health 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): International Normalised Ratio Increased 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.
Wytens Side Effect Report#7604918-8
Oedema Genital, Nephrotic Syndrome, Oedema Peripheral
This report suggests a potential Wytens Oedema Genital 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. After starting Wytens the patient began experiencing various side effects, including: Oedema Genital, Nephrotic Syndrome, Oedema PeripheralAdditional 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.
Wytens Side Effect Report#5414920-2
Anaemia Haemolytic Autoimmune, Antiphospholipid Syndrome, Coombs Positive Haemolytic Anaemia, Cytolytic Hepatitis, Double Stranded Dna Antibody, Hyperproteinaemia, Systemic Lupus Erythematosus
This Anaemia Haemolytic Autoimmune 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 using 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 ErythematosusThe 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.
Wytens Side Effect Report#5343410-0
Condition Aggravated, Diabetes Mellitus, Fatigue, Systemic Lupus Erythematosus
This Condition Aggravated side effect was reported by a consumer or non-health professional from France. A 65-year-old female patient (weight:NA) experienced the following symptoms/conditions: hypertension.The patient was prescribed Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate) (drug dosage: Oral), which was initiated on
Jan 01, 2004. Concurrently used drugs: NA..After starting to take Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate) the consumer reported adverse symptoms, such as: Condition Aggravated, Diabetes Mellitus, Fatigue, Systemic Lupus ErythematosusThese side effects may potentially be related to Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate).
Wytens Side Effect Report#5275636-9
Amnesia, Delirium, Memory Impairment, Road Traffic Accident
This is a report of a 56-year-old male patient (weight: NA) from Japan, suffering from the following health symptoms/conditions: NA, who was treated with Wytens (dosage: 2 Mg, start time:
Aug 02, 2003), combined with:
  • Diovan (80 Mg)
  • Myslee (10 Mg)
and developed a serious reaction and side effect(s): Amnesia, Delirium, Memory Impairment, Road Traffic Accident after the beginning of treatment. This case can indicate the possible existence of increased vulnerability to Wytens treatment in male patients, resulting in Amnesia side effect.
Wytens Side Effect Report#4906311-5
Eczema
This report suggests a potential Wytens /spa/ Eczema side effect(s) that can have serious consequences. A 75-year-old male patient (weight: NA) from France was diagnosed with the following symptoms/conditions: NA and used Wytens /spa/ (dosage: NA) starting NS. After starting Wytens /spa/ the patient began experiencing various side effects, including: EczemaAdditional drugs used concurrently:
  • Befizal
  • Allopurinol
  • Xanax
  • Tareg (160 Mg, Qd)
Although Wytens /spa/ demonstrated significant improvements in a number of clinically relevant cases, troublesome symptoms, such as Eczema, may still occur.
Wytens Side Effect Report#4699649-0
Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Carotid Artery Atheroma, Cerebrovascular Accident, Loss Of Consciousness, Renal Failure Acute
This Blood Lactate Dehydrogenase Increased problem was reported by a consumer or non-health professional from . A 58-year-old male patient (weight: NA) was diagnosed with the following symptoms/conditions: NA. On NS this consumer started treatment with Wytens (bisoprolol/hydrochlorothiazide, Tablet, 0) (dosage: See Image). The following drugs were being taken at the same time:
  • Valsartan (160 Mg 1x Per 1 Day Oral)
  • Daonin (glibenclamide)
  • Di-actane (naftidrofuryl Oxalate)
  • Allopurinol
  • Plavix
When using Wytens (bisoprolol/hydrochlorothiazide, Tablet, 0), the patient experienced the following unwanted symptoms/side effects: Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Carotid Artery Atheroma, Cerebrovascular Accident, Loss Of Consciousness, Renal Failure AcuteThe 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 Blood Lactate Dehydrogenase Increased, may become evident only after a product is in use by the general population.
Wytens Side Effect Report#4695982-7
Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Blood Urea Increased, Cerebrovascular Accident, Glycosylated Haemoglobin Increased, Loss Of Consciousness, Malaise, Proteinuria
This Blood Creatinine Increased side effect was reported by a consumer or non-health professional from . A 58-year-old male patient (weight:NA) experienced the following symptoms/conditions: NA.The patient was prescribed Wytens (drug dosage: 10 Mg, Qd), which was initiated on NS. Concurrently used drugs:
  • Daonil
  • Di-actane (200 Mg, Bid)
  • Allopurinol (200 Mg, Qd)
  • Tareg (160 Mg, Qd)
  • Plavix (75 Mg, Qd)
.After starting to take Wytens the consumer reported adverse symptoms, such as: Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Blood Urea Increased, Cerebrovascular Accident, Glycosylated Haemoglobin Increased, Loss Of Consciousness, Malaise, ProteinuriaThese side effects may potentially be related to Wytens. The patient was hospitalized.



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.

Ask a Doctor Online
12 Doctors are Online.
A Question is Answered Every 9 Seconds!
Ask a Doctor >

Track Your Side Effects

Note Your Observations

It is really important to keep track of your health 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

    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.

    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.

    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.

    Ask a Doctor Online
    12 Doctors are Online.
    A Question is Answered Every 9 Seconds!
    Ask a Doctor >

    Discuss Wytens Side Effects

    Did You Have a Wytens Side Effect?

    Yes, Severe
    Yes, Moderate
    Yes, Minor
    No

    How Effective is Wytens for You?

    Exceeded Expectations
    Effective
    Somewhat Effective
    Not Effective

    Wytens Safety Alerts, Active Ingredients, Usage Information

    More About Wytens

    Side Effects reported to FDA: 8

    Wytens safety alerts: No

    Reported hospitalizations: 1

    Latest Wytens clinical trials