TENORMIN Side Effects

7001158-0 | Bradycardia, Cardiac Arrest
on Sep 16, 2010 Female patient from JAPAN , 71 years of age, weighting 116.8 lb, was diagnosed with atrial fibrillation (What is atrial fibrillation?), hypertension, dyslipidaemia, upper respiratory tract inflammation and was treated with Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, cardiac arrest (What is cardiac arrest?). Tenormin dosage: . During the same period patient was treated with PRONON (View Pronon Review and Pronon Label ), ALISRYTHM (50 Mg 1 - 2 Times A Day) (View Alisrythm Review and Alisrythm Label ), AZELASTINE HCL (View Azelastine Hcl Review and Azelastine Hcl Label ), KUBACRON (View Kubacron Review and Kubacron Label ), OLMETEC (View Olmetec Review and Olmetec Label ), LIPITOR (View Lipitor Review and Lipitor Label ), PELEX (View Pelex Review and Pelex Label ).

6988741-3 | Bradycardia, Loss Of Consciousness
Patient was taking Tenormin (View Usage). Patient had the following side effects: bradycardia, loss of consciousness on Sep 13, 2010 from JAPAN Additional patient health information: Female patient , 71 years of age, was diagnosed with hypertension and. Tenormin dosage: . During the same period patient was treated with PRONON (View Pronon Review and Pronon Label ), SUNRYTHM (50-150 Mg/day) (View Sunrythm Review and Sunrythm Label ).

6976028-4 | Acquired Haemophilia With Anti Fviii, Xi, Or Xiii
Adverse event was reported on Sep 07, 2010 by a Female patient taking Tenormin (View Usage) (Dosage: ) . Location: JAPAN , 80 years of age, weighting 83.78 lb, After Tenormin was administered, patient had the following side effects: acquired haemophilia with anti fviii, xi, or xiii. During the same period patient was treated with CLOTIAZEPAM (View Clotiazepam Review and Clotiazepam Label ), TEPRENONE (View Teprenone Review and Teprenone Label ), PENFILL 50R (View Penfill 50r Review and Penfill 50r Label ).

6960161-7 | Heart Rate Increased, Myocardial Infarction
on Aug 23, 2010 Male patient from AUSTRALIA , 69 years of age, weighting 210.1 lb, was diagnosed with hypertension, palpitations, hypercholesterolaemia and was treated with Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: heart rate increased, myocardial infarction. Tenormin dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ).


6954912-5 | Acquired Haemophilia With Anti Fviii, Xi, Or Xiii
on Aug 25, 2010 Female patient from JAPAN , 80 years of age, weighting 83.78 lb, was treated with Tenormin (View Usage). Patient had the following side effects: acquired haemophilia with anti fviii, xi, or xiii. Tenormin dosage: . During the same period patient was treated with CLOTIAZEPAM (View Clotiazepam Review and Clotiazepam Label ), TEPRENONE (View Teprenone Review and Teprenone Label ), PENFILL 50R (View Penfill 50r Review and Penfill 50r Label ).

6936012-3 | Bradycardia, Dizziness, Hyperhidrosis, Hypertension, Type I Hypersensitivity
Patient was taking Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: bradycardia, dizziness (What is dizziness?), hyperhidrosis, hypertension, type i hypersensitivity on Aug 12, 2010 from SWITZERLAND Additional patient health information: Male patient , 65 years of age, was diagnosed with essential hypertension, psoriatic arthropathy, type 2 diabetes mellitus, hyperlipidaemia, benign prostatic hyperplasia and. Tenormin dosage: . During the same period patient was treated with ACTEMRA (View Actemra Review and Actemra Label ), APROVEL (View Aprovel Review and Aprovel Label ), COVERSUM (View Coversum Review and Coversum Label ), ASPIRINE (View Aspirine Review and Aspirine Label ), GLUCOPHAGE (View Glucophage Review and Glucophage Label ), EZETIMIBE/SIMVASTATIN (Daily) (View Ezetimibe/simvastatin Review and Ezetimibe/simvastatin Label ), XATRAL UNO (View Xatral Uno Review and Xatral Uno Label ).

6935840-8 | Cardiac Arrest
Adverse event was reported on Aug 10, 2010 by a Female patient taking Tenormin (View Usage) (Dosage: 50 Mg, Unk) was diagnosed with hypertension, anaesthesia, maintenance of anaesthesia and. Location: JAPAN , 66 years of age, weighting 99.21 lb, Patient experienced the following unwanted or unexpected effects: cardiac arrest (What is cardiac arrest?). During the same period patient was treated with ULTIVA (0.25 Ug/kg/min) (View Ultiva Review and Ultiva Label ), PROPOFOL (50 Mg, Unk) (View Propofol Review and Propofol Label ), ROCURONIUM BROMIDE (35 Mg, Unk) (View Rocuronium Bromide Review and Rocuronium Bromide Label ), SEVOFLURANE (1.5 %, Unk) (View Sevoflurane Review and Sevoflurane Label ), OXYGEN (40 %, Unk) (View Oxygen Review and Oxygen Label ). Patient was hospitalized.

6924997-0 | Cholestasis, Cytolytic Hepatitis, Hepatic Failure, Jaundice
on Aug 05, 2010 Female patient from FRANCE , 76 years of age, was treated with Tenormin (View Usage). Patient had the following side effects: cholestasis, cytolytic hepatitis, hepatic failure, jaundice (What is jaundice?). Tenormin dosage: . During the same period patient was treated with FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), METFORMIN (View Metformin Review and Metformin Label ), NIDREL (View Nidrel Review and Nidrel Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), AMAREL (View Amarel Review and Amarel Label ), KARDEGIC (View Kardegic Review and Kardegic Label ). Patient was hospitalized.

6847436-7 | Retroperitoneal Fibrosis, Venous Stenosis
on Jul 07, 2010 Male patient from JAPAN , 59 years of age, weighting 176.4 lb, was diagnosed with hypertension and was treated with Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: retroperitoneal fibrosis, venous stenosis. Tenormin dosage: . Patient was hospitalized.

6826037-0 | Retroperitoneal Fibrosis, Venous Stenosis
Patient was taking Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: retroperitoneal fibrosis, venous stenosis on Jun 30, 2010 from JAPAN Additional patient health information: Male patient , 59 years of age, weighting 176.4 lb, was diagnosed with hypertension and. Tenormin dosage: . Patient was hospitalized.

6779139-1 | Bradycardia, Paraesthesia, Speech Disorder
Adverse event was reported on Jun 09, 2010 by a Male patient taking Tenormin (View Usage) (Dosage: ) . Location: SWITZERLAND , 30 years of age, Patient had the following side effects: bradycardia, paraesthesia, speech disorder. Patient was hospitalized.

6735524-5 | Cardio-respiratory Arrest
on May 17, 2010 Female patient from FRANCE , 73 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and was treated with Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: cardio-respiratory arrest. Tenormin dosage: . During the same period patient was treated with CIPRALAN (View Cipralan Review and Cipralan Label ), CORDARONE (View Cordarone Review and Cordarone Label ), COVERSYL (View Coversyl Review and Coversyl Label ), OMACOR (View Omacor Review and Omacor Label ).

6731818-8 | Fall, Pubis Fracture
on May 10, 2010 Female patient from FRANCE , 79 years of age, was treated with Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: fall (What is fall?), pubis fracture. Tenormin dosage: . During the same period patient was treated with DI ANTALVIC (View Di Antalvic Review and Di Antalvic Label ), CACIT VITAMIN D3 (View Cacit Vitamin D3 Review and Cacit Vitamin D3 Label ), FOSAVANCE (View Fosavance Review and Fosavance Label ), LOVENOX (View Lovenox Review and Lovenox Label ). Patient was hospitalized.

6700120-2 | Hepatic Enzyme Increased, Hepatotoxicity
Patient was taking Tenormin (View Usage). Patient had the following side effects: hepatic enzyme increased, hepatotoxicity on Apr 21, 2010 from CANADA Additional patient health information: Female patient , 53 years of age, weighting 140.0 lb, . Tenormin dosage: . During the same period patient was treated with RAZA MIAN (View Raza Mian Review and Raza Mian Label ).

6688116-0 | Hypoglycaemic Coma
Adverse event was reported on Apr 15, 2010 by a Male patient taking Tenormin (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 58 years of age, weighting 74.96 lb, After Tenormin was administered, patient had the following side effects: hypoglycaemic coma.

6686202-2 | Depression, Depression Suicidal
on Apr 13, 2010 Female patient from BELGIUM , child 6 years of age, weighting 44.09 lb, was treated with Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: depression (What is depression?), depression suicidal. Tenormin dosage: .

6679825-8 | Hypertension
on Dec 02, 2009 Female patient from UNITED STATES , 47 years of age, was treated with Tenormin (View Usage). Patient had the following side effects: hypertension. Tenormin dosage: . During the same period patient was treated with ZESTRIL (View Zestril Review and Zestril Label ).

6679822-2 | Blood Pressure Fluctuation, Blood Pressure Increased, Palpitations
Patient was taking Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: blood pressure fluctuation, blood pressure increased, palpitations on Nov 16, 2009 from UNITED STATES Additional patient health information: Female patient , 87 years of age, weighting 110.0 lb, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and. Tenormin dosage: . During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ), ROLAIDS (View Rolaids Review and Rolaids Label ), ECOTRIN (View Ecotrin Review and Ecotrin Label ), OMEGA 3 OIL (View Omega 3 Oil Review and Omega 3 Oil Label ), VITAMIN TAB (View Vitamin Tab Review and Vitamin Tab Label ), CALCIUM (View Calcium Review and Calcium Label ).

6679819-2 | Hypertension
Adverse event was reported on Nov 16, 2009 by a Male patient taking Tenormin (View Usage) (Dosage: ) . Location: UNITED STATES , 45 years of age, Patient experienced the following unwanted or unexpected effects: hypertension.

6679818-0 | Hypertension
on Nov 13, 2009 Male patient from UNITED STATES , 49 years of age, was treated with Tenormin (View Usage). Patient had the following side effects: hypertension. Tenormin dosage: .

6679813-1 | Hypertension
on Nov 17, 2009 Female patient from UNITED STATES , 51 years of age, was treated with Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: hypertension. Tenormin dosage: .

6679808-8 | Ill-defined Disorder
Patient was taking Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: ill-defined disorder on Feb 08, 2010 from UNITED STATES Additional patient health information: Female patient , 83 years of age, . Tenormin dosage: .

6679807-6 | Lung Disorder, Oral Disorder, Tongue Disorder
Adverse event was reported on Feb 19, 2009 by a Female patient taking Tenormin (View Usage) (Dosage: ) . Location: UNITED STATES , 70 years of age, weighting 142.0 lb, Patient had the following side effects: lung disorder, oral disorder, tongue disorder. During the same period patient was treated with TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), XANAX (View Xanax Review and Xanax Label ), CALCIUM (View Calcium Review and Calcium Label ), VITAMIN E (View Vitamin E Review and Vitamin E Label ), FLAXSEED OIL (View Flaxseed Oil Review and Flaxseed Oil Label ), PROTONIX (View Protonix Review and Protonix Label ), AMBIEN (View Ambien Review and Ambien Label ), HYDRALAZINE HCL (View Hydralazine Hcl Review and Hydralazine Hcl Label ).

6679804-0 | Hypertension
on Nov 16, 2009 Male patient from UNITED STATES , 43 years of age, was treated with Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: hypertension. Tenormin dosage: .

6679803-9 | Hypersensitivity
on Jun 03, 2009 Female patient from UNITED STATES , 80 years of age, was treated with Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: hypersensitivity. Tenormin dosage: . During the same period patient was treated with TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), CRESTOR (View Crestor Review and Crestor Label ).

6679800-3 | Anxiety, Dysphagia, Dyspnoea, Ill-defined Disorder, Joint Swelling, Oedema Peripheral, Palpitations, Rash, Weight Increased
Patient was taking Tenormin (View Usage). Patient had the following side effects: anxiety (What is anxiety?), dysphagia, dyspnoea, ill-defined disorder, joint swelling, oedema peripheral, palpitations, rash (What is rash?), weight increased on Feb 10, 2009 from UNITED STATES Additional patient health information: Female patient , 70 years of age, weighting 179.9 lb, was diagnosed with hypertension, palpitations and. Tenormin dosage: 50 Mg In Am / 100 Mg In Pm. During the same period patient was treated with GLUCOTROL (View Glucotrol Review and Glucotrol Label ), LASIX (View Lasix Review and Lasix Label ).

6679796-4 | Hypertension
Adverse event was reported on Nov 16, 2009 by a Female patient taking Tenormin (View Usage) (Dosage: ) . Location: UNITED STATES , 44 years of age, After Tenormin was administered, patient had the following side effects: hypertension.

6679793-9 | Abdominal Pain Upper, Asthenia, Fatigue, Ill-defined Disorder
on Feb 17, 2009 Female patient from UNITED STATES , 85 years of age, was diagnosed with tachycardia, hypertension and was treated with Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, asthenia, fatigue, ill-defined disorder. Tenormin dosage: . During the same period patient was treated with HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PRAVACHOL (View Pravachol Review and Pravachol Label ), ANTIBIOTIC (View Antibiotic Review and Antibiotic Label ).

6679788-5 | Hypertension
on Nov 16, 2009 Female patient from UNITED STATES , 47 years of age, was treated with Tenormin (View Usage). Patient had the following side effects: hypertension. Tenormin dosage: .

6679784-8 | Heart Rate Decreased
Patient was taking Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: heart rate decreased on Sep 22, 2009 from UNITED STATES Additional patient health information: Female patient , 65 years of age, . Tenormin dosage: . During the same period patient was treated with LYRICA (View Lyrica Review and Lyrica Label ), CYMBALTA (View Cymbalta Review and Cymbalta Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ), XANAX (View Xanax Review and Xanax Label ), DARVOCET N 100 (View Darvocet-n 100 Review and Darvocet-n 100 Label ), PREMARIN (View Premarin Review and Premarin Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ), CREON (View Creon Review and Creon Label ).

6679781-2 | Asthenia, Malaise, Restlessness
Adverse event was reported on Apr 20, 2009 by a Male patient taking Tenormin (View Usage) (Dosage: ) . Location: UNITED STATES , 54 years of age, Patient experienced the following unwanted or unexpected effects: asthenia, malaise, restlessness.

6679776-9 | Blood Pressure Increased, Heart Rate Increased, Paraesthesia
on Sep 18, 2009 Female patient from UNITED STATES , 73 years of age, weighting 149.9 lb, was treated with Tenormin (View Usage). Patient had the following side effects: blood pressure increased, heart rate increased, paraesthesia. Tenormin dosage: .

6679772-1 | Hypertension
on Nov 16, 2009 Female patient from UNITED STATES , 50 years of age, was treated with Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: hypertension. Tenormin dosage: .

6679770-8 | Fatigue, Hypercalcaemia, Hyperparathyroidism, Nephrolithiasis, Parathyroidectomy
Patient was taking Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: fatigue, hypercalcaemia, hyperparathyroidism, nephrolithiasis, parathyroidectomy on Aug 12, 2009 from UNITED STATES Additional patient health information: Female patient , 70 years of age, weighting 190.0 lb, was diagnosed with hypertension and. Tenormin dosage: . During the same period patient was treated with VASOTEC (View Vasotec Review and Vasotec Label ), UROCIT K (View Urocit-k Review and Urocit-k Label ), SUPPLEMENTS (View Supplements Review and Supplements Label ), CALCIUM (View Calcium Review and Calcium Label ).

6679767-8 | Ageusia
Adverse event was reported on Dec 30, 2009 by a Female patient taking Tenormin (View Usage) (Dosage: ) . Location: UNITED STATES , 72 years of age, weighting 132.1 lb, Patient had the following side effects: ageusia. During the same period patient was treated with ZICAM (View Zicam Review and Zicam Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), MEDROL (View Medrol Review and Medrol Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), BONIVA (View Boniva Review and Boniva Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ), CALCIUM (View Calcium Review and Calcium Label ).

6679764-2 | Hypertension
on Nov 17, 2009 Male patient from UNITED STATES , 45 years of age, was treated with Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: hypertension. Tenormin dosage: .

6679763-0 | Hypertension
on Nov 16, 2009 Male patient from UNITED STATES , 42 years of age, was treated with Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: hypertension. Tenormin dosage: .

6679760-5 | Hypertension
Patient was taking Tenormin (View Usage). Patient had the following side effects: hypertension on Nov 16, 2009 from UNITED STATES Additional patient health information: Male patient , 46 years of age, . Tenormin dosage: .

6679759-9 | Hypertension
Adverse event was reported on Nov 16, 2009 by a Male patient taking Tenormin (View Usage) (Dosage: ) . Location: UNITED STATES , 42 years of age, After Tenormin was administered, patient had the following side effects: hypertension.

6678821-4 | Fall, Orthostatic Hypotension
on Apr 06, 2010 Female patient from FRANCE , 73 years of age, weighting 119.3 lb, was diagnosed with renal transplant and was treated with Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: fall (What is fall?), orthostatic hypotension. Tenormin dosage: . During the same period patient was treated with AMLOR (View Amlor Review and Amlor Label ), AMIODARONE HCL (View Amiodarone Hcl Review and Amiodarone Hcl Label ), LASIX (View Lasix Review and Lasix Label ), NEXIUM (View Nexium Review and Nexium Label ), CERTICAN (View Certican Review and Certican Label ), NEORAL (View Neoral Review and Neoral Label ), OROCAL D3 (View Orocal D3 Review and Orocal D3 Label ). Patient was hospitalized.

6671130-9 | Ankle Fracture, Convulsion, Disorientation, Fall, Head Injury, Loss Of Consciousness
on Apr 01, 2010 Female patient from FRANCE , 88 years of age, was diagnosed with hypertension, dementia (What is dementia?), hypothyroidism and was treated with Tenormin (View Usage). Patient had the following side effects: ankle fracture, convulsion, disorientation, fall (What is fall?), head injury, loss of consciousness. Tenormin dosage: . During the same period patient was treated with ARICEPT (View Aricept Review and Aricept Label ), ELISOR (View Elisor Review and Elisor Label ), LEVOTHYROX (View Levothyrox Review and Levothyrox Label ). Patient was hospitalized.

6670676-7 | Convulsion, Heart Rate Decreased, Tachycardia
Patient was taking Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: convulsion, heart rate decreased, tachycardia on Mar 30, 2010 from UNITED STATES Additional patient health information: Male patient , 78 years of age, weighting 142.0 lb, was diagnosed with heart rate irregular and. Tenormin dosage: . During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), IODIPINE (View Iodipine Review and Iodipine Label ). Patient was hospitalized.

6657281-3 | Hypoglycaemic Coma
Adverse event was reported on Mar 24, 2010 by a Male patient taking Tenormin (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 58 years of age, Patient experienced the following unwanted or unexpected effects: hypoglycaemic coma.

6655499-7 | Syncope
on Mar 18, 2010 Female patient from SPAIN , 68 years of age, was diagnosed with phaeochromocytoma, anxiety (What is anxiety?), osteoarthritis (What is osteoarthritis?) and was treated with Tenormin (View Usage). Patient had the following side effects: syncope. Tenormin dosage: . During the same period patient was treated with CARDURA (4 Mg (1/2 -0-1/2)) (View Cardura Review and Cardura Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), CONDROSAN (View Condrosan Review and Condrosan Label ). Patient was hospitalized.

6645819-1 | Convulsion
on Mar 15, 2010 Female patient from FRANCE , 88 years of age, was diagnosed with hypertension, dementia (What is dementia?), hypothyroidism and was treated with Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: convulsion. Tenormin dosage: . During the same period patient was treated with ARICEPT (View Aricept Review and Aricept Label ), ELISOR (View Elisor Review and Elisor Label ), LEVOTHYROX (View Levothyrox Review and Levothyrox Label ). Patient was hospitalized.

6633972-5 | Aplastic Anaemia
Patient was taking Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: aplastic anaemia on Mar 08, 2010 from FRANCE Additional patient health information: Male patient , 32 years of age, . Tenormin dosage: . During the same period patient was treated with TAMOXIFEN CITRATE (View Tamoxifen Citrate Review and Tamoxifen Citrate Label ), TRIATEC (View Triatec Review and Triatec Label ), AMLOR (View Amlor Review and Amlor Label ), OFLOCET (View Oflocet Review and Oflocet Label ), VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), TIENAM (View Tienam Review and Tienam Label ), SPECIAFOLDINE (View Speciafoldine Review and Speciafoldine Label ), NEORECORMON (View Neorecormon Review and Neorecormon Label ). Patient was hospitalized.

6580283-2 | Depression, Depression Suicidal
Adverse event was reported on Feb 03, 2010 by a Female patient taking Tenormin (View Usage) (Dosage: ) . Location: BELGIUM , child 6 years of age, weighting 44.09 lb, Patient had the following side effects: depression (What is depression?), depression suicidal.

6579393-5 | Fall
on Feb 03, 2010 Female patient from FRANCE , 89 years of age, was diagnosed with hypertension, type 2 diabetes mellitus and was treated with Tenormin (View Usage). After Tenormin was administered, patient had the following side effects: fall (What is fall?). Tenormin dosage: . During the same period patient was treated with COVERSYL (View Coversyl Review and Coversyl Label ), DIAMICRON (View Diamicron Review and Diamicron Label ), ELISOR (View Elisor Review and Elisor Label ), KARDEGIC (View Kardegic Review and Kardegic Label ). Patient was hospitalized.

6576673-4 | Retroperitoneal Fibrosis
on Feb 02, 2010 Male patient from JAPAN , 73 years of age, was treated with Tenormin (View Usage). Patient experienced the following unwanted or unexpected effects: retroperitoneal fibrosis. Tenormin dosage: .

6576670-9 | Hallucination, Auditory, Memory Impairment
Patient was taking Tenormin (View Usage). Patient had the following side effects: hallucination, auditory, memory impairment on Feb 01, 2010 from FRANCE Additional patient health information: Male patient , 37 years of age, . Tenormin dosage: . During the same period patient was treated with NEORAL (View Neoral Review and Neoral Label ), CELLCEPT (View Cellcept Review and Cellcept Label ), SOLUPRED (View Solupred Review and Solupred Label ), AMLOR (View Amlor Review and Amlor Label ), EZTROL (View Eztrol Review and Eztrol Label ), VASTEN (View Vasten Review and Vasten Label ), MIRCERA (View Mircera Review and Mircera Label ), APROVEL (View Aprovel Review and Aprovel Label ). Patient was hospitalized.