Wytens Side Effects|
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Wytens Adverse Effect Reports (FDA)
International Normalised Ratio Increased (7893482-4)
on Oct 04, 2011 Male patient from JAPAN , weighting 132.3 lb, was diagnosed with
Patient was taking other medications:
Oedema Genital, Nephrotic Syndrome, Oedema Peripheral (7604918-8)
Patient was taking Wytens (View Usage). Patient had the following side effects: oedema genital, nephrotic syndrome, oedema peripheral on Jun 29, 2011 from JAPAN Additional patient health information: Male patient , 68 years of age, . Wytens dosage: N/A.
Patient was taking other medications:
Anaemia Haemolytic Autoimmune, Antiphospholipid Syndrome, Coombs Positive Haemolytic Anaemia, Cytolytic Hepatitis, Double Stranded Dna Antibody, Hyperproteinaemia, Systemic Lupus Erythematosus (5414920-2)
Adverse event was reported on Jul 26, 2007 by a Female patient taking Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate) (View Usage) (Dosage: Oral) was diagnosed with
Patient was taking other medications:
Condition Aggravated, Diabetes Mellitus, Fatigue, Systemic Lupus Erythematosus (5343410-0)
on May 21, 2007 Female patient from FRANCE , 65 years of age, was diagnosed with
Amnesia, Delirium, Memory Impairment, Road Traffic Accident (5275636-9)
on Mar 14, 2007 Male patient from JAPAN , 56 years of age, was treated with Wytens(View Usage). Patient had the following side effects: amnesia, delirium, memory impairment, road traffic accident. Wytens dosage: 2 Mg.
Patient was taking other medications:
Eczema (4906311-5)
Patient was taking Wytens /spa/ (View Usage). After Wytens was administered, patient had the following side effects: eczema (What is eczema?) on Feb 02, 2006 from FRANCE Additional patient health information: Male patient , 75 years of age, . Wytens /spa/ dosage: N/A.
Patient was taking other medications:
Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Carotid Artery Atheroma, Cerebrovascular Accident, Loss Of Consciousness, Renal Failure Acute (4699649-0)
Adverse event was reported on Jun 16, 2005 by a Male patient taking Wytens (bisoprolol/hydrochlorothiazide, Tablet, 0) (View Usage) (Dosage: See Image) . Location: , 58 years of age, Patient experienced the following unwanted or unexpected effects: blood lactate dehydrogenase increased, blood triglycerides increased, carotid artery atheroma, cerebrovascular accident, loss of consciousness, renal failure acute.
Patient was taking other medications:
Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Blood Urea Increased, Cerebrovascular Accident, Glycosylated Haemoglobin Increased, Loss Of Consciousness, Malaise, Proteinuria (4695982-7)
on Jun 14, 2005 Male patient from , 58 years of age, weighting 185.2 lb, was treated with Wytens (View Usage). Patient had the following 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.
Patient was taking other medications:
on Oct 04, 2011 Male patient from JAPAN , weighting 132.3 lb, was diagnosed with
- hypertension
- atrial fibrillation (What is atrial fibrillation?)
Patient was taking other medications:
- PRADAXA (220 Mg) (View Pradaxa Review and Pradaxa Label )
- AMLODIPINE (5 Mg) (View Amlodipine Review and Amlodipine Label )
- DIOVAN (80 Mg) (View Diovan Review and Diovan Label )
- DOXAZON (2 Mg) (View Doxazon Review and Doxazon Label )
- KALLIKREIN (30 Mg) (View Kallikrein Review and Kallikrein Label )
Oedema Genital, Nephrotic Syndrome, Oedema Peripheral (7604918-8)
Patient was taking Wytens (View Usage). Patient had the following side effects: oedema genital, nephrotic syndrome, oedema peripheral on Jun 29, 2011 from JAPAN Additional patient health information: Male patient , 68 years of age, . Wytens dosage: N/A.
Patient was taking other medications:
- CORINAEL (View Corinael Review and Corinael Label )
- PAMILCON (View Pamilcon Review and Pamilcon Label )
- LIPITOR (View Lipitor Review and Lipitor Label )
- LANTUS (View Lantus Review and Lantus Label )
- CILOSTAZOL (View Cilostazol Review and Cilostazol Label )
- DIOVAN (View Diovan Review and Diovan Label )
Anaemia Haemolytic Autoimmune, Antiphospholipid Syndrome, Coombs Positive Haemolytic Anaemia, Cytolytic Hepatitis, Double Stranded Dna Antibody, Hyperproteinaemia, Systemic Lupus Erythematosus (5414920-2)
Adverse event was reported on Jul 26, 2007 by a Female patient taking Wytens (tablet) (hydrochlorothiazide, Bisoprolol Fumarate) (View Usage) (Dosage: Oral) was diagnosed with
- hypertension
Patient was taking other medications:
- RABEPRAZOLE SODIUM (Oral) (View Rabeprazole Sodium Review and Rabeprazole Sodium Label )
- XANAX (0,125 Mg (0,1125 Mg, 1 In 1 D) Oral) (View Xanax Review and Xanax Label )
Condition Aggravated, Diabetes Mellitus, Fatigue, Systemic Lupus Erythematosus (5343410-0)
on May 21, 2007 Female patient from FRANCE , 65 years of age, was diagnosed with
- hypertension
Amnesia, Delirium, Memory Impairment, Road Traffic Accident (5275636-9)
on Mar 14, 2007 Male patient from JAPAN , 56 years of age, was treated with Wytens(View Usage). Patient had the following side effects: amnesia, delirium, memory impairment, road traffic accident. Wytens dosage: 2 Mg.
Patient was taking other medications:
- DIOVAN (80 Mg) (View Diovan Review and Diovan Label )
- MYSLEE (10 Mg) (View Myslee Review and Myslee Label )
Eczema (4906311-5)
Patient was taking Wytens /spa/ (View Usage). After Wytens was administered, patient had the following side effects: eczema (What is eczema?) on Feb 02, 2006 from FRANCE Additional patient health information: Male patient , 75 years of age, . Wytens /spa/ dosage: N/A.
Patient was taking other medications:
- BEFIZAL (View Befizal Review and Befizal Label )
- ALLOPURINOL (View Allopurinol Review and Allopurinol Label )
- XANAX (View Xanax Review and Xanax Label )
- TAREG (160 Mg, Qd) (View Tareg Review and Tareg Label )
Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Carotid Artery Atheroma, Cerebrovascular Accident, Loss Of Consciousness, Renal Failure Acute (4699649-0)
Adverse event was reported on Jun 16, 2005 by a Male patient taking Wytens (bisoprolol/hydrochlorothiazide, Tablet, 0) (View Usage) (Dosage: See Image) . Location: , 58 years of age, Patient experienced the following unwanted or unexpected effects: blood lactate dehydrogenase increased, blood triglycerides increased, carotid artery atheroma, cerebrovascular accident, loss of consciousness, renal failure acute.
Patient was taking other medications:
- VALSARTAN (160 Mg 1x Per 1 Day Oral) (View Valsartan Review and Valsartan Label )
- DAONIN (GLIBENCLAMIDE) (View Daonin (glibenclamide) Review and Daonin (glibenclamide) Label )
- DI ACTANE (NAFTIDROFURYL OXALATE) (View Di-actane (naftidrofuryl Oxalate) Review and Di-actane (naftidrofuryl Oxalate) Label )
- ALLOPURINOL (View Allopurinol Review and Allopurinol Label )
- PLAVIX (View Plavix Review and Plavix Label )
Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Triglycerides Increased, Blood Urea Increased, Cerebrovascular Accident, Glycosylated Haemoglobin Increased, Loss Of Consciousness, Malaise, Proteinuria (4695982-7)
on Jun 14, 2005 Male patient from , 58 years of age, weighting 185.2 lb, was treated with Wytens (View Usage). Patient had the following 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.
Patient was taking other medications:
- DAONIL (View Daonil Review and Daonil Label )
- DI ACTANE (200 Mg, Bid) (View Di-actane Review and Di-actane Label )
- ALLOPURINOL (200 Mg, Qd) (View Allopurinol Review and Allopurinol Label )
- TAREG (160 Mg, Qd) (View Tareg Review and Tareg Label )
- PLAVIX (75 Mg, Qd) (View Plavix Review and Plavix Label )
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Side Effects reported to FDA: 8. View All Wytens safety alerts: No Reported hospitalizations: 1 |