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Wytens Side Effects

Report Wytens Side Effects

If you experienced any harmful or unwanted effects of Wytens, please share your experience. This could help to raise awareness about Wytens side effects, identify uknown risks and inform health professionals and patients taking Wytens.

Examples: headache, dizziness



View a complete list of Wytens side effects or compare Wytens side effects

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 (eg, physician, pharmacist). Your health care provider can provide additional clinical information and complete a copy of the side effect reporting form.

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.

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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
on Oct 04, 2011 Male from JAPAN , weighting 132.3 lb, was diagnosed with and was treated with Wytens. Directly after, patient experienced the unwanted or unexpected Wytens side effects: international normalised ratio increased. Wytens dosage: 2 Mg.
Associated medications used:
  • Pradaxa (220 Mg)
  • Amlodipine (5 Mg)
  • Diovan (80 Mg)
  • Doxazon (2 Mg)
  • Kallikrein (30 Mg)


Oedema Genital, Nephrotic Syndrome, Oedema Peripheral
Patient was taking Wytens. Patient felt the following Wytens side effects: oedema genital, nephrotic syndrome, oedema peripheral on Jun 29, 2011 from JAPAN Additional patient health information: Male , 68 years of age, . Wytens dosage: N/A.
Multiple prescriptions taken:
  • Corinael
  • Pamilcon
  • Lipitor
  • Lantus
  • Cilostazol
  • Diovan


Anaemia Haemolytic Autoimmune, Antiphospholipid Syndrome, Coombs Positive Haemolytic Anaemia, Cytolytic Hepatitis, Double Stranded Dna Antibody, Hyperproteinaemia, Systemic Lupus Erythematosus
Adverse event was reported on Jul 26, 2007 by a Female taking Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate) (Dosage: Oral) was diagnosed with and. Location: FRANCE , 71 years of age, After Wytens was administered, patient encountered several Wytens side effects: anaemia haemolytic autoimmune, antiphospholipid syndrome, coombs positive haemolytic anaemia, cytolytic hepatitis, double stranded dna antibody, hyperproteinaemia, systemic lupus erythematosus.
Multiple concurrent drugs taken:
  • Rabeprazole Sodium (Oral)
  • Xanax (0,125 Mg (0,1125 Mg, 1 In 1 D) Oral)
Patient was hospitalized.

Condition Aggravated, Diabetes Mellitus, Fatigue, Systemic Lupus Erythematosus
on May 21, 2007 Female from FRANCE , 65 years of age, was diagnosed with and was treated with Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate). Directly after, patient experienced the unwanted or unexpected Wytens side effects: condition aggravated, diabetes mellitus, fatigue, systemic lupus erythematosus. Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate) dosage: Oral.


Amnesia, Delirium, Memory Impairment, Road Traffic Accident
on Mar 14, 2007 Male from JAPAN , 56 years of age, was treated with Wytens. Patient felt the following Wytens side effects: amnesia, delirium, memory impairment, road traffic accident. Wytens dosage: 2 Mg.
Multiple prescriptions taken:
  • Diovan (80 Mg)
  • Myslee (10 Mg)


Eczema
Patient was taking Wytens /spa/. After Wytens was administered, patient encountered several Wytens side effects: eczema on Feb 02, 2006 from FRANCE Additional patient health information: Male , 75 years of age, . Wytens /spa/ dosage: N/A.
Multiple concurrent drugs taken:
  • 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
Adverse event was reported on Jun 16, 2005 by a Male taking Wytens (bisoprolol/hydrochlorothiazide, Tablet, 0) (Dosage: See Image) . Location: , 58 years of age, Directly after, patient experienced the unwanted or unexpected Wytens side effects: blood lactate dehydrogenase increased, blood triglycerides increased, carotid artery atheroma, cerebrovascular accident, loss of consciousness, renal failure acute.
Associated medications used:
  • Valsartan (160 Mg 1x Per 1 Day Oral)
  • Daonin (glibenclamide)
  • Di-actane (naftidrofuryl Oxalate)
  • Allopurinol
  • Plavix
Patient was hospitalized.

Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Blood Urea Increased, Cerebrovascular Accident, Glycosylated Haemoglobin Increased, Loss Of Consciousness, Malaise, Proteinuria
on Jun 14, 2005 Male from , 58 years of age, weighting 185.2 lb, was treated with Wytens. Patient felt the following Wytens side effects: blood creatinine increased, blood lactate dehydrogenase increased, blood triglycerides increased, blood urea increased, cerebrovascular accident, glycosylated haemoglobin increased, loss of consciousness, malaise, proteinuria. Wytens dosage: 10 Mg, Qd.
Multiple prescriptions taken:
  • Daonil
  • Di-actane (200 Mg, Bid)
  • Allopurinol (200 Mg, Qd)
  • Tareg (160 Mg, Qd)
  • Plavix (75 Mg, Qd)
Patient was hospitalized.

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


    Track Online

  • User Sign In
  • Register to track your side effects

  • 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

    Did You Have a Wytens Side Effect?

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    How Effective is Wytens for You?

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    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