LOTENSIN Side Effects

6815167-5 | Cough
on Jun 30, 2010 Female patient from UNITED STATES , 45 years of age, weighting 250.0 lb, was diagnosed with hypertension and was treated with Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: cough. Lotensin dosage: 20/12.5 Qd Po.

6568692-9 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Back Pain, Body Temperature Increased, Face Oedema, Hypertension, Nasopharyngitis, Nephritic Syndrome
Patient was taking Lotensin (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, back pain (What is back pain?), body temperature increased, face oedema, hypertension, nasopharyngitis, nephritic syndrome on Jan 25, 2010 from CHINA Additional patient health information: Male patient , 55 years of age, was diagnosed with hypertension and. Lotensin dosage: 1 Df, Qd. During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6438887-3 | Hypotension
Adverse event was reported on Nov 03, 2009 by a Male patient taking Lotensin (View Usage) (Dosage: ) was diagnosed with nephropathy and. Location: CHINA , 60 years of age, After Lotensin was administered, patient had the following side effects: hypotension.

6316078-4 | Confusional State, Dehydration, Headache, Oedema Peripheral, Pain In Extremity, Renal Failure
on Aug 11, 2009 Female patient from UNITED STATES , 59 years of age, was treated with Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: confusional state, dehydration, headache (What is headache?), oedema peripheral, pain in extremity, renal failure. Lotensin dosage: 20 Mg, Unk. During the same period patient was treated with LOTENSIN HCT (20mg) (View Lotensin Hct Review and Lotensin Hct Label ), NORVASC (5mg, Unk) (View Norvasc Review and Norvasc Label ). Patient was hospitalized.


6290719-2 | Biopsy Stomach, Cough, Feeling Abnormal, Haemoptysis, Vomiting
on Jul 28, 2009 Female patient from UNITED STATES , weighting 190.0 lb, was diagnosed with hypertension and was treated with Lotensin (View Usage). Patient had the following side effects: biopsy stomach, cough, feeling abnormal, haemoptysis, vomiting. Lotensin dosage: 20 Mg 1 X Po.

6163489-6 | Blood Glucose Decreased, Erythema, Swelling Face
Patient was taking Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: blood glucose decreased, erythema, swelling face on Jan 31, 2002 from UNITED STATES Additional patient health information: Female patient , 61 years of age, weighting 173.0 lb, was diagnosed with essential hypertension, accidental exposure, blood cholesterol, diabetes mellitus and. Lotensin dosage: . During the same period patient was treated with ANDROGEL (Daily Dose: Unk.) (View Androgel Review and Androgel Label ), LIPITOR (View Lipitor Review and Lipitor Label ), EVISTA (View Evista Review and Evista Label ), ACTOS (View Actos Review and Actos Label ), GLUCOVANCE (View Glucovance Review and Glucovance Label ).

6161837-4 | Alopecia
Adverse event was reported on Sep 25, 2008 by a Female patient taking Lotensin (View Usage) (Dosage: Daily Dose: 40 Milligram(s)) was diagnosed with hypertension, accidental exposure and. Location: UNITED STATES , weighting 160.9 lb, Patient experienced the following unwanted or unexpected effects: alopecia. During the same period patient was treated with ANDROGEL (Daily Dose: 5 Gram(s) Via Pump) (View Androgel Review and Androgel Label ).

6127388-8 | Gingival Hyperplasia
on Mar 13, 2009 Male patient from CHINA , 42 years of age, was diagnosed with hypertension and was treated with Lotensin (View Usage). Patient had the following side effects: gingival hyperplasia. Lotensin dosage: 10 Mg, Qd. During the same period patient was treated with LAMIVUDINE (View Lamivudine Review and Lamivudine Label ), MEDROL (View Medrol Review and Medrol Label ).

5900276-5 | Abdominal Discomfort, Abdominal Distension, Anorexia, Appetite Disorder, Biliary Dilatation, Biliary Tract Disorder, Blood Pressure Increased, Cholangiolitis, Cholecystitis
on Sep 19, 2008 Male patient from CHINA , 64 years of age, was diagnosed with myocardial infarction and was treated with Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: abdominal discomfort, abdominal distension, anorexia, appetite disorder, biliary dilatation, biliary tract disorder, blood pressure increased, cholangiolitis, cholecystitis. Lotensin dosage: 5 Mg, Qd. Patient was hospitalized.

5585307-7 | Abortion Induced
Patient was taking Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: abortion induced on Dec 20, 2007 from CHINA Additional patient health information: Female patient , 26 years of age, was diagnosed with hypertension and. Lotensin dosage: 10 Mg/day.

5499621-7 | Impaired Driving Ability, Road Traffic Accident, Somnambulism
Adverse event was reported on May 20, 2007 by a Male patient taking Lotensin (View Usage) (Dosage: Unk) was diagnosed with hypertension, insomnia, depression (What is depression?) and. Location: UNITED STATES , weighting 179.9 lb, Patient had the following side effects: impaired driving ability, road traffic accident, somnambulism. During the same period patient was treated with AMBIEN (View Ambien Review and Ambien Label ), ALCOHOL (Unk) (View Alcohol Review and Alcohol Label ), PROZAC (View Prozac Review and Prozac Label ).

5494158-3 | Cyanosis, Erythema, Peripheral Coldness, Rash Papular, Raynaud's Phenomenon
on Oct 16, 2007 Male patient from CHINA , 87 years of age, weighting 110.2 lb, was diagnosed with hypertension and was treated with Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: cyanosis, erythema, peripheral coldness, rash papular, raynaud's phenomenon. Lotensin dosage: 10 Mg, Qd. During the same period patient was treated with ASMETON (View Asmeton Review and Asmeton Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ). Patient was hospitalized.

5492769-2 | Asthenia, Chest Pain, Microalbuminuria, Pain In Jaw, Palpitations, Proteinuria, White Blood Cell Count Decreased
on Oct 15, 2007 Female patient from UNITED STATES , 59 years of age, was diagnosed with hypertension, diabetes mellitus, hyperlipidaemia and was treated with Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, chest pain (What is chest pain?), microalbuminuria, pain in jaw, palpitations, proteinuria, white blood cell count decreased. Lotensin dosage: 40 Mg, Qd. During the same period patient was treated with LOTREL (Unk, Qd) (View Lotrel Review and Lotrel Label ), ASPIRIN (81 Mg, Bid) (View Aspirin Review and Aspirin Label ), HUMALOG (Various Doses, Ac) (View Humalog Review and Humalog Label ), VYTORIN (10/20mg, Qd) (View Vytorin Review and Vytorin Label ), LANTUS (56 U, Qd) (View Lantus Review and Lantus Label ).

5486288-7 | Heart Rate Decreased
Patient was taking Lotensin (View Usage). Patient had the following side effects: heart rate decreased on Oct 08, 2007 from CHINA Additional patient health information: Male patient , 38 years of age, was diagnosed with hypertension and. Lotensin dosage: 10 Mg, Qd. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), JIN KUI SHEN QI PILL (View Jin Kui Shen Qi Pill Review and Jin Kui Shen Qi Pill Label ).

5479156-8 | Coronary Artery Disease, Myocardial Infarction, Percutaneous Coronary Intervention, Pharyngeal Oedema, Stent Placement, Tongue Oedema
Adverse event was reported on Oct 01, 2007 by a Male patient taking Lotensin (View Usage) (Dosage: 40 Mg, Bid) was diagnosed with hypertension, coronary artery disease (What is coronary artery disease?) and. Location: UNITED STATES , 65 years of age, weighting 218.0 lb, After Lotensin was administered, patient had the following side effects: coronary artery disease (What is coronary artery disease?), myocardial infarction, percutaneous coronary intervention, pharyngeal oedema, stent placement, tongue oedema. During the same period patient was treated with BENAZEPRIL HYDROCHLORIDE (40 Mg, Bid) (View Benazepril Hydrochloride Review and Benazepril Hydrochloride Label ), GLUCOVANCE (5/5000, Bid) (View Glucovance Review and Glucovance Label ), BYETTA (10 Ug, Bid) (View Byetta Review and Byetta Label ), ACTOS (15 Mg, Qd) (View Actos Review and Actos Label ), LEVEMIR (15 U, Qhs) (View Levemir Review and Levemir Label ), VALIUM (5 Mg, 1-2 Qd) (View Valium Review and Valium Label ), PLAVIX (75 Mg, Qd) (View Plavix Review and Plavix Label ), LIPITOR (80 Mg, Qd) (View Lipitor Review and Lipitor Label ).

5470492-8 | Myocardial Infarction, Pharyngeal Oedema, Tongue Oedema
on Sep 15, 2007 Male patient from UNITED STATES , 65 years of age, was treated with Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial infarction, pharyngeal oedema, tongue oedema. Lotensin dosage: . During the same period patient was treated with BENAZEPRIL HYDROCHLORIDE (View Benazepril Hydrochloride Review and Benazepril Hydrochloride Label ).

5460142-9 | Tongue Oedema
on Jun 19, 2007 Female patient from UNITED STATES , 64 years of age, was diagnosed with hypertension and was treated with Lotensin (View Usage). Patient had the following side effects: tongue oedema. Lotensin dosage: See Image.

5460123-5 | Benign Prostatic Hyperplasia, Fall, Syncope
Patient was taking Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: benign prostatic hyperplasia, fall (What is fall?), syncope on Jun 14, 2007 from UNITED STATES Additional patient health information: Male patient , 85 years of age, was diagnosed with benign prostatic hyperplasia and. Lotensin dosage: Oral. During the same period patient was treated with FLOMAX (0.4 Mg, Qd, Oral) (View Flomax Review and Flomax Label ), HYDROCHLOROTHIAZIDE (Oral) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

5460115-6 | Blood Pressure Fluctuation, Flushing, Hyperhidrosis
Adverse event was reported on May 01, 2007 by a Female patient taking Lotensin (View Usage) (Dosage: See Image) was diagnosed with hypertension and. Location: UNITED STATES , 63 years of age, Patient experienced the following unwanted or unexpected effects: blood pressure fluctuation, flushing, hyperhidrosis. During the same period patient was treated with XANAX (View Xanax Review and Xanax Label ), VITAMINS (NO INGREDIENTS/SUBSTANCES) (View Vitamins (no Ingredients/substances) Review and Vitamins (no Ingredients/substances) Label ).

5452201-1 | Cardiac Operation
on Sep 07, 2007 Female patient from UNITED STATES , 49 years of age, was diagnosed with hypertension and was treated with Lotensin (View Usage). Patient had the following side effects: cardiac operation. Lotensin dosage: Unk, Bid.

5391276-5 | Gait Disturbance, Musculoskeletal Stiffness
on May 31, 2007 Male patient from CHINA , 68 years of age, weighting 121.3 lb, was diagnosed with hypertension and was treated with Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: gait disturbance, musculoskeletal stiffness. Lotensin dosage: 10 Mg, Qd.

5387343-2 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Bilirubin Increased, Gamma-glutamyltransferase Increased, Urine Bilirubin Increased, Urine Protein/creatinine Ratio Increased
Patient was taking Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, gamma-glutamyltransferase increased, urine bilirubin increased, urine protein/creatinine ratio increased on Jul 04, 2007 from CHINA Additional patient health information: Male patient , 49 years of age, was diagnosed with hypertension and. Lotensin dosage: 10 Mg, Qd. During the same period patient was treated with ADALAT (View Adalat Review and Adalat Label ).

5375939-3 | Angioedema, Oedema Mouth, Swollen Tongue
Adverse event was reported on Jun 27, 2007 by a Male patient taking Lotensin (View Usage) (Dosage: 10mg Tablet Daily Po) was diagnosed with hypertension and. Location: UNITED STATES , 77 years of age, weighting 155.9 lb, Patient had the following side effects: angioedema, oedema mouth, swollen tongue. Patient was hospitalized.

5373476-3 | Angioedema, Cardiac Failure Congestive, Myocardial Infarction, Pneumonia
on Jun 26, 2007 Male patient from UNITED STATES , 72 years of age, weighting 194.0 lb, was diagnosed with blood pressure (What is blood pressure?) and was treated with Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: angioedema, cardiac failure congestive, myocardial infarction, pneumonia (What is pneumonia?). Lotensin dosage: 40mg Daily Po. Patient was hospitalized.

5371555-8 | Angioedema
on Jun 25, 2007 Male patient from UNITED STATES , 64 years of age, weighting 164.0 lb, was diagnosed with hypertension and was treated with Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: angioedema. Lotensin dosage: Unsure. Patient was hospitalized.

5350475-9 | Gait Disturbance, Musculoskeletal Stiffness
Patient was taking Lotensin (View Usage). Patient had the following side effects: gait disturbance, musculoskeletal stiffness on May 31, 2007 from CHINA Additional patient health information: Male patient , 68 years of age, weighting 121.3 lb, . Lotensin dosage: 10 Mg, Qd.

5316830-8 | Abdominal Pain, Blood Creatine Phosphokinase Increased, Decreased Appetite, Hepatocellular Damage, Influenza Like Illness, Nausea, Ocular Icterus, Prothrombin Time Prolonged, Urine Colour Abnormal
Adverse event was reported on May 01, 2007 by a Male patient taking Lotensin (View Usage) (Dosage: Unk D/f, Unk) was diagnosed with depression (What is depression?) and. Location: UNITED STATES , 47 years of age, weighting 255.0 lb, After Lotensin was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), blood creatine phosphokinase increased, decreased appetite, hepatocellular damage, influenza like illness, nausea (What is nausea?), ocular icterus, prothrombin time prolonged, urine colour abnormal. During the same period patient was treated with NEXIUM (40 Mg, Unk) (View Nexium Review and Nexium Label ), ZYRTEC (10 Mg, Daily (1/d)) (View Zyrtec Review and Zyrtec Label ), CYMBALTA (60 Mg, Daily (1/d)) (View Cymbalta Review and Cymbalta Label ), LIPITOR (20 Mg, Daily (1/d)) (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

5300751-0 | Impaired Driving Ability, Road Traffic Accident, Sleep Walking
on Mar 12, 2007 Male patient from UNITED STATES , 50 years of age, was diagnosed with insomnia and was treated with Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: impaired driving ability, road traffic accident, sleep walking. Lotensin dosage: Unk. During the same period patient was treated with AMBIEN (View Ambien Review and Ambien Label ), ALCOHOL (Unk) (View Alcohol Review and Alcohol Label ).

5295270-4 | Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Creatine Phosphokinase Increased, Decreased Appetite, Influenza Like Illness, Jaundice
on Apr 10, 2007 Male patient from UNITED STATES , 47 years of age, weighting 255.0 lb, was diagnosed with depression (What is depression?) and was treated with Lotensin (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood creatine phosphokinase increased, decreased appetite, influenza like illness, jaundice (What is jaundice?). Lotensin dosage: Unk D/f, Unk. During the same period patient was treated with NEXIUM (40 Mg, Unk) (View Nexium Review and Nexium Label ), ZYRTEC (10 Mg, Daily (1/d)) (View Zyrtec Review and Zyrtec Label ), CYMBALTA (60 Mg, Daily (1/d)) (View Cymbalta Review and Cymbalta Label ), LIPITOR (20 Mg, Daily (1/d)) (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

5259009-0 | Caesarean Section, Normal Newborn
Patient was taking Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: caesarean section, normal newborn on Feb 26, 2007 from CHINA Additional patient health information: Female patient , 28 years of age, was diagnosed with nephropathy and. Lotensin dosage: 10 Mg, Qd.

5243611-6 | Lip Swelling
Adverse event was reported on Feb 20, 2007 by a Female patient taking Lotensin (View Usage) (Dosage: ) . Location: UNITED STATES , 57 years of age, Patient experienced the following unwanted or unexpected effects: lip swelling.

5231453-7 | Aphasia, Back Pain, Cerebrovascular Accident, Drooling, Dysarthria, Fall, Hypertension, Hypoaesthesia Facial, Limb Injury
on Jan 26, 2007 Female patient from UNITED STATES , 61 years of age, weighting 244.7 lb, was diagnosed with hypertension, hypothyroidism and was treated with Lotensin (View Usage). Patient had the following side effects: aphasia (What is aphasia?), back pain (What is back pain?), cerebrovascular accident, drooling, dysarthria, fall (What is fall?), hypertension, hypoaesthesia facial, limb injury. Lotensin dosage: 5 Mg, Qd. During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ). Patient was hospitalized.

5188096-3 | Angioneurotic Oedema, Swollen Tongue
on Dec 14, 2006 Female patient from UNITED STATES , 69 years of age, was diagnosed with hypertension and was treated with Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: angioneurotic oedema, swollen tongue. Lotensin dosage: 40 Mg Po Qday. During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), GEMFIBROZIL (View Gemfibrozil Review and Gemfibrozil Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), PREMARIN (View Premarin Review and Premarin Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), DARVOCET (View Darvocet Review and Darvocet Label ), LEVOXYL (View Levoxyl Review and Levoxyl Label ), COMBIVENT (View Combivent Review and Combivent Label ). Patient was hospitalized.

5180940-9 | Acute Coronary Syndrome, Dysarthria, Hypotension, Lethargy
Patient was taking Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: acute coronary syndrome, dysarthria, hypotension, lethargy on Dec 14, 2006 from UNITED STATES Additional patient health information: Male patient , 65 years of age, was diagnosed with blood pressure (What is blood pressure?) and. Lotensin dosage: Po 10mg. Patient was hospitalized.

5173730-4 | Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Creatine Phosphokinase Increased, Decreased Appetite, Influenza Like Illness, Jaundice
Adverse event was reported on Oct 27, 2006 by a Male patient taking Lotensin (View Usage) (Dosage: Unk D/f, Unk) was diagnosed with depression (What is depression?) and. Location: UNITED STATES , 47 years of age, weighting 255.0 lb, Patient had the following side effects: abdominal pain (What is abdominal pain?), alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood creatine phosphokinase increased, decreased appetite, influenza like illness, jaundice (What is jaundice?). During the same period patient was treated with NEXIUM (40 Mg, Unk) (View Nexium Review and Nexium Label ), ZYRTEC (10 Mg, Daily (1/d)) (View Zyrtec Review and Zyrtec Label ), CYMBALTA (60 Mg, Daily (1/d)) (View Cymbalta Review and Cymbalta Label ), LIPITOR (20 Mg, Daily (1/d)) (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

5161034-5 | Cough, Dyspnoea, Laryngeal Oedema, Laryngeal Stenosis, Nasopharyngitis, Tracheoscopy Abnormal
on Sep 28, 2006 Male patient from CHINA , 43 years of age, was diagnosed with lupus nephritis and was treated with Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: cough, dyspnoea, laryngeal oedema, laryngeal stenosis, nasopharyngitis, tracheoscopy abnormal. Lotensin dosage: 10 Mg/day. During the same period patient was treated with PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ).

5144799-8 | Back Pain, Cerebrovascular Accident, Drooling, Dysarthria, Fall, Hypertension, Limb Injury
on Oct 25, 2006 Female patient from UNITED STATES , 61 years of age, was diagnosed with hypertension, hypothyroidism and was treated with Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: back pain (What is back pain?), cerebrovascular accident, drooling, dysarthria, fall (What is fall?), hypertension, limb injury. Lotensin dosage: 5 Mg, Qd. During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ). Patient was hospitalized.

5134352-4 | Cough, Dyspnoea, Laryngeal Oedema, Laryngeal Stenosis, Nasopharyngitis, Tracheoscopy Abnormal
Patient was taking Lotensin (View Usage). Patient had the following side effects: cough, dyspnoea, laryngeal oedema, laryngeal stenosis, nasopharyngitis, tracheoscopy abnormal on Sep 28, 2006 from CHINA Additional patient health information: Male patient , 43 years of age, was diagnosed with lupus nephritis and. Lotensin dosage: 10 Mg/day. During the same period patient was treated with PREDNISONE (View Prednisone Review and Prednisone Label ).

5133497-2 | Cough, Dyspnoea, Laryngeal Oedema, Laryngeal Stenosis, Nasopharyngitis, Tracheoscopy Abnormal
Adverse event was reported on Sep 28, 2006 by a Male patient taking Lotensin (View Usage) (Dosage: 10 Mg/day) was diagnosed with lupus nephritis and. Location: CHINA , 43 years of age, After Lotensin was administered, patient had the following side effects: cough, dyspnoea, laryngeal oedema, laryngeal stenosis, nasopharyngitis, tracheoscopy abnormal. During the same period patient was treated with PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ).

4971032-X | Hepatic Enzyme Increased
on Apr 11, 2006 Male patient from UNITED STATES , 42 years of age, weighting 300.0 lb, was diagnosed with hypertension and was treated with Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: hepatic enzyme increased. Lotensin dosage: 10mg Twice Daily Po. During the same period patient was treated with HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), ZOLOFT (View Zoloft Review and Zoloft Label ).

4964448-9 | Amputation, Anaemia Of Chronic Disease, Blood Creatinine Increased, Blood Glucose Increased, Blood Pressure Systolic Increased, Blood Urea Increased, Constipation, Creatinine Renal Clearance Decreased, Dermatitis Atopic
on Jan 05, 2006 Female patient from UNITED STATES , 41 years of age, weighting 164.0 lb, was diagnosed with hypertension and was treated with Lotensin (View Usage). Patient had the following side effects: amputation, anaemia of chronic disease, blood creatinine increased, blood glucose increased, blood pressure systolic increased, blood urea increased, constipation (What is constipation?), creatinine renal clearance decreased, dermatitis atopic. Lotensin dosage: 40 Mg, Qd. During the same period patient was treated with FUROSEMIDE (40 Mg, Bid) (View Furosemide Review and Furosemide Label ), MULTIVITAMIN (View Multivitamin Review and Multivitamin Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ), AMITRIPTYLINE (25 Mg, Prn) (View Amitriptyline Review and Amitriptyline Label ), INSULIN (View Insulin Review and Insulin Label ), NORVASC (5 Mg, Qd) (View Norvasc Review and Norvasc Label ), LANTUS (View Lantus Review and Lantus Label ). Patient was hospitalized.

4889192-8 | Angioneurotic Oedema
Patient was taking Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: angioneurotic oedema on Jan 20, 2006 from UNITED STATES Additional patient health information: Male patient , 48 years of age, was diagnosed with hypertension and. Lotensin dosage: . Patient was hospitalized.

4886588-5 | Amputation, Anaemia Of Chronic Disease, Blood Creatinine Increased, Blood Glucose Increased, Blood Pressure Inadequately Controlled, Blood Pressure Systolic Increased, Blood Urea Increased, Constipation, Creatinine Renal Clearance Decreased
Adverse event was reported on Jan 05, 2006 by a Female patient taking Lotensin (View Usage) (Dosage: 40 Mg, Qd) was diagnosed with hypertension and. Location: UNITED STATES , 41 years of age, weighting 164.0 lb, Patient experienced the following unwanted or unexpected effects: amputation, anaemia of chronic disease, blood creatinine increased, blood glucose increased, blood pressure inadequately controlled, blood pressure systolic increased, blood urea increased, constipation (What is constipation?), creatinine renal clearance decreased. During the same period patient was treated with FUROSEMIDE (40 Mg, Bid) (View Furosemide Review and Furosemide Label ), MULTIVITAMIN (View Multivitamin Review and Multivitamin Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ), AMITRIPTYLINE HCL (25 Mg, Prn) (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), INSULIN (View Insulin Review and Insulin Label ), NORVASC (5 Mg, Qd) (View Norvasc Review and Norvasc Label ), LANTUS (View Lantus Review and Lantus Label ). Patient was hospitalized.

4883396-6 | Cardiac Failure Congestive, Dyspnoea, Fatigue, Fluid Retention, Palpitations
on Jan 11, 2006 Female patient from UNITED STATES , 68 years of age, was diagnosed with hypertension and was treated with Lotensin (View Usage). Patient had the following side effects: cardiac failure congestive, dyspnoea, fatigue, fluid retention, palpitations. Lotensin dosage: 5 Mg, Qd. Patient was hospitalized.

4865319-9 | Angioneurotic Oedema, Upper Airway Resistance Syndrome
on Dec 21, 2005 Female patient from UNITED STATES , 77 years of age, weighting 202.8 lb, was diagnosed with hypertension and was treated with Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: angioneurotic oedema, upper airway resistance syndrome. Lotensin dosage: 10 Mg Daily Po. Patient was hospitalized.

4801552-X | Pruritus, Urticaria
Patient was taking Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: pruritus, urticaria on Oct 11, 2005 from UNITED STATES Additional patient health information: Male patient , 44 years of age, weighting 168.0 lb, was diagnosed with hypercholesterolaemia, hypertension and. Lotensin dosage: 20 Mg Po One Daily. During the same period patient was treated with ZOCOR (20 Mg Po One Daily) (View Zocor Review and Zocor Label ), BENAZEPRIL HCL (View Benazepril Hcl Review and Benazepril Hcl Label ).

4798105-9 | Atrial Fibrillation, Blood Potassium Increased, Renal Failure Acute
Adverse event was reported on Oct 12, 2005 by a Male patient taking Lotensin (View Usage) (Dosage: 20 Mg Po Qd [prior To Admission]) was diagnosed with hypertension and. Location: UNITED STATES , weighting 165.0 lb, Patient had the following side effects: atrial fibrillation (What is atrial fibrillation?), blood potassium increased, renal failure acute. During the same period patient was treated with PRAVACHOL (View Pravachol Review and Pravachol Label ), HYTRIN (View Hytrin Review and Hytrin Label ), EFFEXOR XR (View Effexor Xr Review and Effexor Xr Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ), ARICEPT (View Aricept Review and Aricept Label ), PLAVIX (View Plavix Review and Plavix Label ). Patient was hospitalized.

4770790-7 | Angioneurotic Oedema, Chest Discomfort
on Sep 14, 2005 Male patient from UNITED STATES , 63 years of age, was diagnosed with coronary artery atherosclerosis, hypertension and was treated with Lotensin (View Usage). After Lotensin was administered, patient had the following side effects: angioneurotic oedema, chest discomfort. Lotensin dosage: Po. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), EZETIMIBE (View Ezetimibe Review and Ezetimibe Label ), DILTIAZEM (View Diltiazem Review and Diltiazem Label ). Patient was hospitalized.

4754187-1 | Application Site Dermatitis, Chromaturia, Dizziness, Fatigue, Hypersensitivity, Nausea, Oropharyngeal Swelling, Rash, Rash Macular
on Apr 20, 2005 Female patient from UNITED STATES , 45 years of age, was diagnosed with hypertension, depression (What is depression?) and was treated with Lotensin (View Usage). Patient experienced the following unwanted or unexpected effects: application site dermatitis, chromaturia, dizziness (What is dizziness?), fatigue, hypersensitivity, nausea (What is nausea?), oropharyngeal swelling, rash (What is rash?), rash macular. Lotensin dosage: Oral. During the same period patient was treated with WELLBUTRIN (View Wellbutrin Review and Wellbutrin Label ), MULTIVITAMINS (ASCORBIC ACID, ERGOCALCIFEROL, FOLIC ACID, NICOTINAMIDE (View Multivitamins (ascorbic Acid, Ergocalciferol, Folic Acid, Nicotinamide Review and Multivitamins (ascorbic Acid, Ergocalciferol, Folic Acid, Nicotinamide Label ), CLARITIN (View Claritin Review and Claritin Label ), VITAMIN B (NO INGREDIENTS/SUBSTANCES) (View Vitamin B (no Ingredients/substances) Review and Vitamin B (no Ingredients/substances) Label ).

4754186-X | Angioneurotic Oedema, Swelling Face
Patient was taking Lotensin (View Usage). Patient had the following side effects: angioneurotic oedema, swelling face on Dec 02, 2004 from UNITED STATES Additional patient health information: Female patient , 77 years of age, was diagnosed with hypertension and. Lotensin dosage: 10 Mg, Qd, Oral. During the same period patient was treated with ATENOLOL TABLETS USP (NGX) (ATENOLOL) TABLET (View Atenolol Tablets Usp (ngx) (atenolol) Tablet Review and Atenolol Tablets Usp (ngx) (atenolol) Tablet Label ), ZOCOR (View Zocor Review and Zocor Label ).