PROPRANOLOL Side Effects

7023682-7 | Hypoglycaemia, Hypoglycaemic Seizure
on Sep 16, 2010 Female patient from GERMANY , child 1 years of age, was diagnosed with haemangioma and was treated with Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: hypoglycaemia, hypoglycaemic seizure. Propranolol dosage: 2 Mg/kg/day In Three Split Doses. Patient was hospitalized.

7022978-2 | Metabolic Acidosis, Overdose, Shock, Temporomandibular Joint Syndrome
Patient was taking Propranolol (View Usage). Patient had the following side effects: metabolic acidosis, overdose, shock, temporomandibular joint syndrome on Sep 15, 2010 from IRAN (ISLAMIC REPUBLIC OF) Additional patient health information: Male patient , 32 years of age, was diagnosed with overdose and. Propranolol dosage: Took 60 X 40mg Tablets. Patient was hospitalized.

7021674-5 | Gait Disturbance, Visual Impairment
Adverse event was reported on Sep 14, 2010 by a Female patient taking Propranolol (View Usage) (Dosage: 20 Df Once; Oral Formulation; Tablet) . Location: FRANCE , 35 years of age, After Propranolol was administered, patient had the following side effects: gait disturbance, visual impairment. During the same period patient was treated with STILNOX (ZOLPIDEN) (View Stilnox (zolpiden) Review and Stilnox (zolpiden) Label ), ESCITALOPRAM (View Escitalopram Review and Escitalopram Label ), TERCIAN (CYAMEMAZINE) (View Tercian (cyamemazine) Review and Tercian (cyamemazine) Label ). Patient was hospitalized.

7021670-8 | Bradycardia, Coma, Fall, Meningorrhagia, Subdural Haemorrhage
on Sep 02, 2010 Male patient from FRANCE , 90 years of age, was diagnosed with essential tremor and was treated with Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, coma, fall (What is fall?), meningorrhagia, subdural haemorrhage. Propranolol dosage: 20 Mg Oral. During the same period patient was treated with ARICEPT (View Aricept Review and Aricept Label ), KARDEGIC (ACETYLSALICYLATE LYSINE) (View Kardegic (acetylsalicylate Lysine) Review and Kardegic (acetylsalicylate Lysine) Label ), POLYETHYLENE GLYCOL (View Polyethylene Glycol Review and Polyethylene Glycol Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), DIAFUSOR (GLYCERYL TRINITRATE) (View Diafusor (glyceryl Trinitrate) Review and Diafusor (glyceryl Trinitrate) Label ), CETORNAN (ORNITHINE OXOGLURATE) (View Cetornan (ornithine Oxoglurate) Review and Cetornan (ornithine Oxoglurate) Label ), OXAZEPAM (View Oxazepam Review and Oxazepam Label ), ESCITALOPRAM (View Escitalopram Review and Escitalopram Label ). Patient was hospitalized.


7021080-3 | Bradycardia, Metabolic Acidosis, Overdose, Shock, Temporomandibular Joint Syndrome
on Sep 15, 2010 Female patient from IRAN (ISLAMIC REPUBLIC OF) , 26 years of age, was diagnosed with overdose and was treated with Propranolol (View Usage). Patient had the following side effects: bradycardia, metabolic acidosis, overdose, shock, temporomandibular joint syndrome. Propranolol dosage: Took 90 X 40mg Tablets. Patient was hospitalized.

7008763-6 | Back Pain, Cholestasis Of Pregnancy, Convulsion, Induced Labour, Premature Labour
Patient was taking Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: back pain (What is back pain?), cholestasis of pregnancy, convulsion, induced labour, premature labour on Sep 07, 2010 from UNITED KINGDOM Additional patient health information: Female patient , 36 years of age, was diagnosed with back pain (What is back pain?), epilepsy (What is epilepsy?) and. Propranolol dosage: . During the same period patient was treated with ARIPIPRAZOLE (View Aripiprazole Review and Aripiprazole Label ), (DIHYDROCODEINE) (30 Mg 1 To 2 Tds) (View (dihydrocodeine) Review and (dihydrocodeine) Label ), LAMICTAL (400 Mg Bid, Oral) (View Lamictal Review and Lamictal Label ), LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), (NORETHISTERONE) STRENGTH: 350UG (View (norethisterone) Strength: 350ug Review and (norethisterone) Strength: 350ug Label ), SERTRALINE HYDROCHLORIDE (100 Mg Bid) (View Sertraline Hydrochloride Review and Sertraline Hydrochloride Label ), (AMOXICILLIN) (View (amoxicillin) Review and (amoxicillin) Label ), BETAMETHASONE (View Betamethasone Review and Betamethasone Label ). Patient was hospitalized.

7001741-2 | Hyperhidrosis, Hypoglycaemic Seizure, Lethargy, Somnolence
Adverse event was reported on Sep 10, 2010 by a Female patient taking Propranolol (View Usage) (Dosage: 2 Mg/kg/day In 3 Split Doses) was diagnosed with haemangioma and. Location: GERMANY , child 1 years of age, Patient experienced the following unwanted or unexpected effects: hyperhidrosis, hypoglycaemic seizure, lethargy, somnolence. During the same period patient was treated with VACCINES (View Vaccines Review and Vaccines Label ). Patient was hospitalized.

6987770-3 | Aplasia, Cardiac Arrest, Convulsion, Diarrhoea, Electrocardiogram Qt Prolonged, Hepatitis Toxic, Loss Of Consciousness, Torsade De Pointes
on Sep 01, 2010 Female patient from FRANCE , 59 years of age, was treated with Propranolol (View Usage). Patient had the following side effects: aplasia, cardiac arrest (What is cardiac arrest?), convulsion, diarrhoea, electrocardiogram qt prolonged, hepatitis toxic, loss of consciousness, torsade de pointes. Propranolol dosage: 160 Mg Oral Formulation: Capsule. During the same period patient was treated with EPIRUBICIN (One Single Dose Intravenous (not Otherwise Specified) Formulation: Injecti) (View Epirubicin Review and Epirubicin Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), LASIX (View Lasix Review and Lasix Label ), SUCRALFATE (View Sucralfate Review and Sucralfate Label ), DIAMICRON (GLICLAZIDE) (View Diamicron (gliclazide) Review and Diamicron (gliclazide) Label ), ACTOS (View Actos Review and Actos Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), ANTIBIOTICS (ANTIBIOTICS) (View Antibiotics (antibiotics) Review and Antibiotics (antibiotics) Label ). Patient was hospitalized.

6987766-1 | Bradycardia, Coma, Fall, Meningorrhagia, Open Wound, Subdural Haematoma
on Sep 02, 2010 Male patient from FRANCE , 90 years of age, was diagnosed with essential tremor and was treated with Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: bradycardia, coma, fall (What is fall?), meningorrhagia, open wound, subdural haematoma. Propranolol dosage: 20 Mg, Oral Formulation. During the same period patient was treated with ARICEPT (View Aricept Review and Aricept Label ), KARDEGIC (ACETYLSALICYLATE LYSINE) (View Kardegic (acetylsalicylate Lysine) Review and Kardegic (acetylsalicylate Lysine) Label ), FORLAX (MACROGEL) (View Forlax (macrogel) Review and Forlax (macrogel) Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), DIAFUSOR (GLYCERYL TRINITRATE) (View Diafusor (glyceryl Trinitrate) Review and Diafusor (glyceryl Trinitrate) Label ), CETORNAN (ORNITHINE OXOGLURATE) (View Cetornan (ornithine Oxoglurate) Review and Cetornan (ornithine Oxoglurate) Label ), OXAZEPAM (View Oxazepam Review and Oxazepam Label ), ESCITALOPRAM (View Escitalopram Review and Escitalopram Label ). Patient was hospitalized.

6982078-4 | Bradycardia, Deformity, Depressed Level Of Consciousness, Hypotension, Joint Dislocation, Metabolic Acidosis, Overdose, Shock
Patient was taking Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, deformity, depressed level of consciousness, hypotension, joint dislocation, metabolic acidosis, overdose, shock on Aug 26, 2010 from IRAN (ISLAMIC REPUBLIC OF) Additional patient health information: Male patient , 32 years of age, . Propranolol dosage: Dose Text: 60 Tablets Of 40 Mg Oral Formulation: Tablet. Patient was hospitalized.

6982077-2 | Blood Calcium Decreased, Blood Potassium Decreased, Bradycardia, Cyanosis, Joint Dislocation, Metabolic Acidosis, Overdose, Salivary Hypersecretion, Shock
Adverse event was reported on Aug 26, 2010 by a Female patient taking Propranolol (View Usage) (Dosage: 40 Mg Daily Oral Formulation: Tablet / Dose Text: 90 Tablets Of 40 Mg Oral Formulation: Tablet) . Location: IRAN (ISLAMIC REPUBLIC OF) , 26 years of age, Patient had the following side effects: blood calcium decreased, blood potassium decreased, bradycardia, cyanosis, joint dislocation, metabolic acidosis, overdose, salivary hypersecretion, shock. Patient was hospitalized.

6981030-2 | Depressed Level Of Consciousness, Hypotension, Joint Dislocation, Metabolic Acidosis, Overdose, Shock
on Sep 06, 2010 Male patient from IRAN (ISLAMIC REPUBLIC OF) , 32 years of age, was treated with Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: depressed level of consciousness, hypotension, joint dislocation, metabolic acidosis, overdose, shock. Propranolol dosage: 60 Df, Once/single. Patient was hospitalized.

6981029-6 | Bradycardia, Cyanosis, Joint Dislocation, Metabolic Acidosis, Overdose, Peripheral Coldness, Radial Pulse Decreased, Salivary Hypersecretion, Shock
on Sep 06, 2010 Female patient from IRAN (ISLAMIC REPUBLIC OF) , 26 years of age, was treated with Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, cyanosis, joint dislocation, metabolic acidosis, overdose, peripheral coldness, radial pulse decreased, salivary hypersecretion, shock. Propranolol dosage: 90 Df, Once/single. Patient was hospitalized.

6973878-5 | Depressed Level Of Consciousness, Hypotension, Ill-defined Disorder, Joint Dislocation, Metabolic Acidosis, Overdose, Shock, Trismus
Patient was taking Propranolol (View Usage). Patient had the following side effects: depressed level of consciousness, hypotension, ill-defined disorder, joint dislocation, metabolic acidosis, overdose, shock, trismus on Aug 31, 2010 from IRAN (ISLAMIC REPUBLIC OF) Additional patient health information: Male patient , 32 years of age, . Propranolol dosage: 60tabs Per Day. Patient was hospitalized.

6970882-8 | Bradycardia, Cyanosis, Ill-defined Disorder, Joint Dislocation, Metabolic Acidosis, Muscle Spasticity, Overdose, Peripheral Coldness
Adverse event was reported on Aug 31, 2010 by a Female patient taking Propranolol (View Usage) (Dosage: 90tab Per Day) . Location: IRAN (ISLAMIC REPUBLIC OF) , 26 years of age, After Propranolol was administered, patient had the following side effects: bradycardia, cyanosis, ill-defined disorder, joint dislocation, metabolic acidosis, muscle spasticity, overdose, peripheral coldness. Patient was hospitalized.

6968989-4 | Brain Injury, Depressed Level Of Consciousness, Epilepsy, Hypersomnia, Hypoglycaemia
on Aug 19, 2010 Female patient from UNITED STATES , child 4 years of age, was diagnosed with tachycardia and was treated with Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: brain injury, depressed level of consciousness, epilepsy (What is epilepsy?), hypersomnia, hypoglycaemia. Propranolol dosage: Daily Dose: .75 Mg / .25 Mg; Intravenous.

6968981-X | Cyanosis, Hyperhidrosis, Hypoglycaemia, Pallor, Stupor
on Aug 19, 2010 Female patient from UNITED STATES , child 1 years of age, was treated with Propranolol (View Usage). Patient had the following side effects: cyanosis, hyperhidrosis, hypoglycaemia, pallor, stupor. Propranolol dosage: Route Of Administration: Oral Formulation.

6968977-8 | Adrenal Insufficiency
Patient was taking Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: adrenal insufficiency on Aug 23, 2010 from UNITED STATES Additional patient health information: Female patient , child 2 years of age, weighting 28.66 lb, . Propranolol dosage: 0.8 Mg/kg, Oral, Every 6 Hours. During the same period patient was treated with LEVOTHYROXINE SODIUM (40 Tablets, Oral, 1 Time) (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), IBUPROFEN (10 Mg/kg, Oral, 1 Time) (View Ibuprofen Review and Ibuprofen Label ). Patient was hospitalized.

6968971-7 | Hyperhidrosis, Hypoglycaemia, Somnolence
Adverse event was reported on Aug 19, 2010 by a Female patient taking Propranolol (View Usage) (Dosage: Route Of Administration: Oral Formulation) . Location: UNITED STATES , child 3 years of age, Patient experienced the following unwanted or unexpected effects: hyperhidrosis, hypoglycaemia, somnolence.

6964066-7 | Decreased Appetite, Headache, Pancreatitis Acute
on Aug 16, 2010 Male patient from FRANCE , 58 years of age, was diagnosed with type 1 diabetes mellitus and was treated with Propranolol (View Usage). Patient had the following side effects: decreased appetite, headache (What is headache?), pancreatitis acute. Propranolol dosage: 40 Mg Daily, Oral Formulation. During the same period patient was treated with NEXIUM (40 Mg Bid, Oral Formulation) (View Nexium Review and Nexium Label ), CRESTOR (10 Mg Daily, Oral Formulation: Tablet) (View Crestor Review and Crestor Label ), TOPIRAMATE (50 Mg Bid, Oral Formulation) (View Topiramate Review and Topiramate Label ), ESCITALOPRAM (20 Mg Daily, Oral Fomulation) (View Escitalopram Review and Escitalopram Label ), CREON (12000 Iu, Oral Formulation) (View Creon Review and Creon Label ), DOGMATIL (SULPIRIDE) (50 Mg Bid, Oral Formulation) (View Dogmatil (sulpiride) Review and Dogmatil (sulpiride) Label ), ACETAMINOPHEN (1 G Tid, Oral Formulation) (View Acetaminophen Review and Acetaminophen Label ), HUMALOG (32 Iu Bid, Subcutaneous Formulation) (View Humalog Review and Humalog Label ). Patient was hospitalized.

6956823-8 | Cardiogenic Shock, Poisoning Deliberate
on Aug 20, 2010 Female patient from FRANCE , 65 years of age, was treated with Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: cardiogenic shock, poisoning deliberate. Propranolol dosage: Oral Formation. During the same period patient was treated with DILTIAZEM (Oral Formation) (View Diltiazem Review and Diltiazem Label ), MIDAZOLAM HCL (Oral Formation) (View Midazolam Hcl Review and Midazolam Hcl Label ), CRESTOR (View Crestor Review and Crestor Label ), METFORMIN (View Metformin Review and Metformin Label ), PROPOFAM (View Propofam Review and Propofam Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

6942318-4 | Hyperhidrosis, Hypoglycaemia, Somnolence
Patient was taking Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: hyperhidrosis, hypoglycaemia, somnolence on Aug 04, 2010 from UNITED STATES Additional patient health information: Female patient , child 3 years of age, . Propranolol dosage: Daily Oral.

6940361-2 | Cyanosis, Hyperhidrosis, Hypoglycaemia, Pallor, Stupor
Adverse event was reported on Aug 04, 2010 by a Female patient taking Propranolol (View Usage) (Dosage: ) . Location: UNITED STATES , child 1 years of age, Patient had the following side effects: cyanosis, hyperhidrosis, hypoglycaemia, pallor, stupor.

6939426-0 | Activities Of Daily Living Impaired, Condition Aggravated, Essential Tremor, Migraine, Orthostatic Hypotension, Seronegative Arthritis, Somnolence, Therapeutic Response Decreased
on Aug 12, 2010 Male patient from CHILE , 72 years of age, was diagnosed with essential tremor and was treated with Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: activities of daily living impaired, condition aggravated, essential tremor, migraine (What is migraine?), orthostatic hypotension, seronegative arthritis, somnolence, therapeutic response decreased. Propranolol dosage: See Image. During the same period patient was treated with PRIMIDONE (250 Mgdaily / 500mg Daily) (View Primidone Review and Primidone Label ), TOPIRAMATE (View Topiramate Review and Topiramate Label ), LEVODOPA (View Levodopa Review and Levodopa Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), MIRTAZAPINE (View Mirtazapine Review and Mirtazapine Label ), LEVETIRACETAM (View Levetiracetam Review and Levetiracetam Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ).

6926030-3 | Disseminated Intravascular Coagulation, Haemodynamic Instability, Neonatal Respiratory Failure, Oedema
on Jul 27, 2010 Female patient from UNITED KINGDOM , child 0 years of age, was diagnosed with supraventricular tachycardia, arrhythmia (What is arrhythmia?) and was treated with Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: disseminated intravascular coagulation, haemodynamic instability, neonatal respiratory failure, oedema. Propranolol dosage: . During the same period patient was treated with DIGITALIS (DIGITALIS PURPUREA) (View Digitalis (digitalis Purpurea) Review and Digitalis (digitalis Purpurea) Label ).

6907655-8 | Aspiration, Asthenia, Cachexia, Cough, Dehydration, Dysphagia, Dysphonia, Hepatic Function Abnormal, Hyperthyroidism
Patient was taking Propranolol (View Usage). Patient had the following side effects: aspiration, asthenia, cachexia, cough, dehydration, dysphagia, dysphonia, hepatic function abnormal, hyperthyroidism on Jul 22, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 74 years of age, was diagnosed with hyperthyroidism and. Propranolol dosage: . During the same period patient was treated with CARBIMAZOLE (View Carbimazole Review and Carbimazole Label ).

6907372-4 | Agitation, Bradycardia, Disorientation, Hyperammonaemia, Metabolic Encephalopathy
Adverse event was reported on Jul 20, 2010 by a Female patient taking Propranolol (View Usage) (Dosage: ) . Location: UNITED KINGDOM , 41 years of age, After Propranolol was administered, patient had the following side effects: agitation, bradycardia, disorientation, hyperammonaemia, metabolic encephalopathy. During the same period patient was treated with CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), FLUPENTIXOL DIHYDROCHLORIDE (View Flupentixol Dihydrochloride Review and Flupentixol Dihydrochloride Label ), OXAZEPAM (View Oxazepam Review and Oxazepam Label ), VALPROATE SODIUM (View Valproate Sodium Review and Valproate Sodium Label ). Patient was hospitalized.

6907371-2 | Arteriosclerosis Coronary Artery, Electrocardiogram St Segment Elevation, Prinzmetal Angina
on Jul 19, 2010 Female patient from FRANCE , 37 years of age, was diagnosed with migraine (What is migraine?) and was treated with Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: arteriosclerosis coronary artery, electrocardiogram st segment elevation, prinzmetal angina. Propranolol dosage: 20 Mg Once, Oral Formulation: Tablet. During the same period patient was treated with ZOMIG (2.5 Mg, Prn, Oral Formulation: Fastmelt) (View Zomig Review and Zomig Label ), RELPAX (View Relpax Review and Relpax Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), VIDORA (INDORAMIN) (View Vidora (indoramin) Review and Vidora (indoramin) Label ), TRIELLA (ETHINYLESTRADIOL, NORETHISTERONE) (View Triella (ethinylestradiol, Norethisterone) Review and Triella (ethinylestradiol, Norethisterone) Label ), ZOLPIDEM TARTRATE (View Zolpidem Tartrate Review and Zolpidem Tartrate Label ), PRAZEPAM (View Prazepam Review and Prazepam Label ). Patient was hospitalized.

6898913-4 | Condition Aggravated, Hepatic Function Abnormal
on Jul 19, 2010 Male patient from UNITED KINGDOM , 74 years of age, weighting 147.7 lb, was diagnosed with hyperthyroidism and was treated with Propranolol (View Usage). Patient had the following side effects: condition aggravated, hepatic function abnormal. Propranolol dosage: . During the same period patient was treated with CARBIMAZOLE (View Carbimazole Review and Carbimazole Label ).

6887586-2 | Neutropenic Sepsis, Oropharyngeal Pain
Patient was taking Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: neutropenic sepsis, oropharyngeal pain on Jul 13, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 18 years of age, was diagnosed with autoimmune thyroiditis and. Propranolol dosage: . During the same period patient was treated with CARBIMAZOLE (View Carbimazole Review and Carbimazole Label ). Patient was hospitalized.

6876826-1 | Neutropenic Sepsis, Oropharyngeal Pain
Adverse event was reported on Jul 13, 2010 by a Male patient taking Propranolol (View Usage) (Dosage: ) was diagnosed with autoimmune thyroiditis and. Location: UNITED KINGDOM , 18 years of age, Patient experienced the following unwanted or unexpected effects: neutropenic sepsis, oropharyngeal pain. During the same period patient was treated with CARBIMAZOLE (View Carbimazole Review and Carbimazole Label ). Patient was hospitalized.

6869506-X | Concussion, Convulsion, Economic Problem, Eye Disorder, Fall, Loss Of Consciousness, Vision Blurred
on Jul 21, 2010 Female patient from UNITED STATES , 18 years of age, weighting 150.0 lb, was diagnosed with migraine prophylaxis and was treated with Propranolol (View Usage). Patient had the following side effects: concussion (What is concussion?), convulsion, economic problem, eye disorder, fall (What is fall?), loss of consciousness, vision blurred. Propranolol dosage: 10 Mg Once A Day Po.

6846981-8 | Anaemia Haemolytic Autoimmune
on Jun 28, 2010 Female patient from FRANCE , 73 years of age, was diagnosed with diabetes mellitus and was treated with Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: anaemia haemolytic autoimmune. Propranolol dosage: 160 Mg Daily/oral. During the same period patient was treated with NEXIUM (40 Mg Bid / 40 Mg Daily/ Oral) (View Nexium Review and Nexium Label ), REPAGLINIDE (Oral) (View Repaglinide Review and Repaglinide Label ), IMOVANE (ZOPICLONE) STRENGTH: 3.75MG (3.75 Mg Daily Oral) (View Imovane (zopiclone) Strength: 3.75mg Review and Imovane (zopiclone) Strength: 3.75mg Label ), XANAX (.25 Mg Daily Oral) (View Xanax Review and Xanax Label ). Patient was hospitalized.

6844799-3 | Neutropenic Sepsis, Oropharyngeal Pain
Patient was taking Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: neutropenic sepsis, oropharyngeal pain on Jul 14, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 18 years of age, was diagnosed with autoimmune thyroiditis and. Propranolol dosage: . During the same period patient was treated with CARBIMAZOLE (View Carbimazole Review and Carbimazole Label ). Patient was hospitalized.

6816941-1 | Dyspnoea, Electrocardiogram Repolarisation Abnormality, Left Ventricular Hypertrophy, Weight Decreased, Weight Increased
Adverse event was reported on Jun 14, 2010 by a Male patient taking Propranolol (View Usage) (Dosage: 160 Mg Oral Forlulation: Capsule Contr Rel) was diagnosed with migraine (What is migraine?), arthralgia and. Location: FRANCE , 49 years of age, Patient had the following side effects: dyspnoea, electrocardiogram repolarisation abnormality, left ventricular hypertrophy, weight decreased, weight increased. During the same period patient was treated with KETOPROFEN (View Ketoprofen Review and Ketoprofen Label ), CELEBREX (View Celebrex Review and Celebrex Label ). Patient was hospitalized.

6796242-0 | Bradycardia
on Jun 24, 2010 Male patient from UNITED STATES , 53 years of age, weighting 145.9 lb, was diagnosed with hypertension and was treated with Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: bradycardia. Propranolol dosage: 120 Mg Every Day Po. Patient was hospitalized.

6785166-0 | Abdominal Pain, Acidosis, Atrioventricular Block Complete, Cardiac Arrest, Collateral Circulation, Dizziness, Dyspnoea, Hypotension
on Jun 09, 2010 Male patient from FRANCE , 60 years of age, was diagnosed with tachycardia and was treated with Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), acidosis, atrioventricular block complete, cardiac arrest (What is cardiac arrest?), collateral circulation, dizziness (What is dizziness?), dyspnoea, hypotension. Propranolol dosage: 40 Mg, Once, Oral. During the same period patient was treated with ISOPTIN (240 Mg, Tablet Er , Daily; Oral) (View Isoptin Review and Isoptin Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ), VASTAREL (TRIMETAZIDINE HYDROCHLORIDE) (View Vastarel (trimetazidine Hydrochloride) Review and Vastarel (trimetazidine Hydrochloride) Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), ALDACTONE (View Aldactone Review and Aldactone Label ).

6785164-7 | Anuria, Cardio-respiratory Arrest, Cardiogenic Shock, Coma, Multi-organ Failure, Supraventricular Tachycardia
Patient was taking Propranolol (View Usage). Patient had the following side effects: anuria, cardio-respiratory arrest, cardiogenic shock, coma, multi-organ failure, supraventricular tachycardia on Jun 04, 2010 from ITALY Additional patient health information: Male patient , 39 years of age, was diagnosed with supraventricular tachycardia and. Propranolol dosage: 2 Mg/dose Text; 5 Mg Infused At Rate Of 0.16 Mg/min Over 30 Minutes; Intravenous.

6773619-0 | Amnesia, Memory Impairment, Muscular Weakness, Musculoskeletal Stiffness
Adverse event was reported on Jun 08, 2010 by a Female patient taking Propranolol (View Usage) (Dosage: 40 Mg; Tid;) was diagnosed with migraine (What is migraine?) and. Location: , 55 years of age, After Propranolol was administered, patient had the following side effects: amnesia, memory impairment, muscular weakness, musculoskeletal stiffness. During the same period patient was treated with RELPAX (View Relpax Review and Relpax Label ).

6772143-9 | Foetal Distress Syndrome, Labile Blood Pressure, Labour Induction, Live Birth
on Jun 07, 2010 Female patient from TAIWAN, PROVINCE OF CHINA , 28 years of age, was diagnosed with ventricular tachycardia and was treated with Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: foetal distress syndrome, labile blood pressure, labour induction, live birth. Propranolol dosage: 10mg Per Day. During the same period patient was treated with MAGNESIUM SULFATE (View Magnesium Sulfate Review and Magnesium Sulfate Label ).

6767246-9 | Bradycardia, Dizziness, Fall, Loss Of Consciousness
on Jun 11, 2010 Male patient from UNITED STATES , 54 years of age, was diagnosed with cardiac failure congestive, hypertension and was treated with Propranolol (View Usage). Patient had the following side effects: bradycardia, dizziness (What is dizziness?), fall (What is fall?), loss of consciousness. Propranolol dosage: 60 Mg Every Day Po. Patient was hospitalized.

6760183-5 | Blood Pressure Systolic Increased, Bradycardia, Loss Of Consciousness, Malaise
Patient was taking Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: blood pressure systolic increased, bradycardia, loss of consciousness, malaise on May 17, 2010 from FRANCE Additional patient health information: Female patient , 86 years of age, was diagnosed with dementia alzheimer's type and. Propranolol dosage: .5 Df Bid / .5 Df Daily, Oral Formulation, Oral. During the same period patient was treated with EXELON (Oral Formulation) (View Exelon Review and Exelon Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), RISPERDAL (View Risperdal Review and Risperdal Label ). Patient was hospitalized.

6758590-X | Raynaud's Phenomenon
Adverse event was reported on May 19, 2010 by a Male patient taking Propranolol (View Usage) (Dosage: 160 Mg Daily Oral) was diagnosed with oesophageal varices haemorrhage and. Location: FRANCE , 63 years of age, Patient experienced the following unwanted or unexpected effects: raynaud's phenomenon. During the same period patient was treated with ATACAND (View Atacand Review and Atacand Label ), (METFORMIN) (View (metformin) Review and (metformin) Label ), DIAMICRON (GLICLAZIDE) (View Diamicron (gliclazide) Review and Diamicron (gliclazide) Label ), ZOLPIDEM TARTRATE (View Zolpidem Tartrate Review and Zolpidem Tartrate Label ). Patient was hospitalized.

6758588-1 | Blood Pressure Increased, Electrocardiogram Qt Prolonged, Loss Of Consciousness, Malaise, Sinus Bradycardia
on May 17, 2010 Female patient from FRANCE , 86 years of age, was diagnosed with dementia alzheimer's type and was treated with Propranolol (View Usage). Patient had the following side effects: blood pressure increased, electrocardiogram qt prolonged, loss of consciousness, malaise, sinus bradycardia. Propranolol dosage: .5 Df Bid / .5 Df Daily Oral / Oral. During the same period patient was treated with EXELON (Oral) (View Exelon Review and Exelon Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), RISPERDAL (View Risperdal Review and Risperdal Label ). Patient was hospitalized.

6733010-X | Atrial Fibrillation, Cardiac Arrest, Coronary Artery Thrombosis, No Therapeutic Response, Pulmonary Embolism, Respiratory Arrest, Visual Acuity Reduced
on May 03, 2010 Female patient from DENMARK , 71 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?), endocrine ophthalmopathy and was treated with Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), cardiac arrest (What is cardiac arrest?), coronary artery thrombosis, no therapeutic response, pulmonary embolism (What is pulmonary embolism?), respiratory arrest, visual acuity reduced. Propranolol dosage: . During the same period patient was treated with METHYLPREDNISOLONE (1 Gm (1 Gm,1 In 1 D), Intravenous) (View Methylprednisolone Review and Methylprednisolone Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), CLOPIDOGREL (View Clopidogrel Review and Clopidogrel Label ), PROPYLTHIOURACIL (View Propylthiouracil Review and Propylthiouracil Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ).

6732736-1 | Aggression, Autoimmune Myocarditis, Basedow's Disease, Blood Pressure Systolic Increased, Cardiac Failure Congestive, Coma, Contusion, Disorientation, Excoriation
Patient was taking Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: aggression, autoimmune myocarditis, basedow's disease, blood pressure systolic increased, cardiac failure congestive, coma, contusion, disorientation, excoriation on Apr 29, 2010 from TAIWAN, PROVINCE OF CHINA Additional patient health information: Female patient , 46 years of age, was diagnosed with thyroid disorder and. Propranolol dosage: 20 Mg Q8ii, Oral Formulation. During the same period patient was treated with DEXAMETHASONE (View Dexamethasone Review and Dexamethasone Label ), PROPYLTHIOURACIL (View Propylthiouracil Review and Propylthiouracil Label ), POTASSIUM IODIDE (View Potassium Iodide Review and Potassium Iodide Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ).

6732728-2 | Aortic Valve Incompetence, Atrioventricular Block, Atrioventricular Block Complete, Blood Pressure Increased, Cardiogenic Shock, Coma, Ejection Fraction Decreased, Mitral Valve Incompetence
Adverse event was reported on May 03, 2010 by a Female patient taking Propranolol (View Usage) (Dosage: 17 Tablets Of 10 Mg, Oral Formulation: Tablet) was diagnosed with hypertension, stress (What is stress?) and. Location: FRANCE , 56 years of age, Patient had the following side effects: aortic valve incompetence, atrioventricular block, atrioventricular block complete, blood pressure increased, cardiogenic shock, coma, ejection fraction decreased, mitral valve incompetence. During the same period patient was treated with TEGRETOL (View Tegretol Review and Tegretol Label ), METFORMAX (METFORMIN HYDROCHLORIDE) (View Metformax (metformin Hydrochloride) Review and Metformax (metformin Hydrochloride) Label ), (ATORVASTATIN) (View (atorvastatin) Review and (atorvastatin) Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ). Patient was hospitalized.

6726006-5 | Brugada Syndrome, Intentional Overdose, Pallor, Suicide Attempt
on Apr 27, 2010 Male patient from FRANCE , 24 years of age, was treated with Propranolol (View Usage). After Propranolol was administered, patient had the following side effects: brugada syndrome, intentional overdose, pallor, suicide attempt. Propranolol dosage: 57 Tablets At A Time, Oral. Patient was hospitalized.

6714534-8 | Brugada Syndrome, Intentional Overdose, Poisoning
on Apr 27, 2010 Female patient from UNITED STATES , 34 years of age, was diagnosed with intentional overdose and was treated with Propranolol (View Usage). Patient experienced the following unwanted or unexpected effects: brugada syndrome, intentional overdose, poisoning (What is poisoning?). Propranolol dosage: Large Amount. Patient was hospitalized.

6713490-6 | Ventricular Extrasystoles
Patient was taking Propranolol (View Usage). Patient had the following side effects: ventricular extrasystoles on Apr 20, 2010 from NORWAY Additional patient health information: Male patient , 17 years of age, . Propranolol dosage: 120 Mg Daily Oral / 180 Mg Daily Oral.