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Summary

FDA Adverse Reports: 163. View All

Vasotec FDA safety alerts: No

Reported deaths: 10

Reported hospitalizations: 67

Vasotec Dosage, Warnings, Usage.

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Weakness, no appetite or thirst, constant coughing.

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Often additional risks of using a medication, such as Vasotec, become known after product is used by a larger number of patients, for a longer period of time, and by patients with different health characteristics from those studied before drug approval. This page allows You to Find answers and discuss health symptoms with other Vasotec users, Learn more about unwanted side effects & find ways to reduce them. Browse Vasotec Adverse Reports reported to FDA and participate in Vasotec discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Vasotec. You can also Post a question to users community or Ask a Doctor. PatientsVille.com is Your Complete Guide to all common, undocumented and undisclosed side effects associated with drugs and vaccines. Browse More Drug Reports Here: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

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Vasotec Adverse Effect Reports (FDA)

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6968392-7 | Cough
on Sep 03, 2010 Female patient from UNITED STATES , weighting 127.0 lb, was treated with Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: cough. Vasotec dosage: .

6963982-X | Dizziness
Patient was taking Vasotec (View Usage). Patient had the following side effects: dizziness (What is dizziness?) on Sep 02, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 220.0 lb, was diagnosed with hypertension and. Vasotec dosage: 5mg 1qd Po.

6929811-5 | Cough
Adverse event was reported on Aug 17, 2010 by a Female patient taking Vasotec (View Usage) (Dosage: 5mg Daily Po) was diagnosed with hypertension and. Location: UNITED STATES , weighting 184.0 lb, After Vasotec was administered, patient had the following side effects: cough.

6825871-0 | Cough, No Therapeutic Response
on Jul 08, 2010 Male patient from UNITED STATES , weighting 228.0 lb, was diagnosed with hypertension and was treated with Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: cough, no therapeutic response. Vasotec dosage: 20 Mg Qd Oral.


6738395-6 | Abasia, Dyspnoea Exertional, Dysstasia, Haemodialysis, Hyperkalaemia, Pain In Extremity
on Apr 19, 2010 Male patient from SLOVENIA , 85 years of age, was diagnosed with cardiac failure and was treated with Vasotec (View Usage). Patient had the following side effects: abasia, dyspnoea exertional, dysstasia, haemodialysis, hyperkalaemia, pain in extremity. Vasotec dosage: 20 Mg Bid Oral. During the same period patient was treated with ALDACTONE /00006201/ (ALDACTONE SPIRONOLACTONE) (25 Mg Qd Oral) (View Aldactone /00006201/ (aldactone - Spironolactone) Review and Aldactone /00006201/ (aldactone - Spironolactone) Label ), AMLOPIN /00972402/ (View Amlopin /00972402/ Review and Amlopin /00972402/ Label ), CORYOL (View Coryol Review and Coryol Label ), ZOCOR (View Zocor Review and Zocor Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized and became disabled.

6735298-8 | Dyspnoea, Swollen Tongue
Patient was taking Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: dyspnoea, swollen tongue on May 20, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 183.0 lb, was diagnosed with hypertension and. Vasotec dosage: 20 Mg Daily Po.

6733003-2 | Abasia, Dyspnoea Exertional, Hyperkalaemia, Pain In Extremity
Adverse event was reported on Apr 29, 2010 by a Male patient taking Vasotec (View Usage) (Dosage: (20 Mg Bid Oral)) was diagnosed with cardiac failure and. Location: SLOVENIA , 85 years of age, Patient experienced the following unwanted or unexpected effects: abasia, dyspnoea exertional, hyperkalaemia, pain in extremity. During the same period patient was treated with ALDACTONE ((25 Mg Qd Oral)) (View Aldactone Review and Aldactone Label ), AMLOPIN /00972402/ (View Amlopin /00972402/ Review and Amlopin /00972402/ Label ), CORYOL (View Coryol Review and Coryol Label ), ZOCOR (View Zocor Review and Zocor Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized and became disabled.

6706094-2 | Cough
on Apr 30, 2010 Male patient from UNITED STATES , weighting 229.0 lb, was treated with Vasotec (View Usage). Patient had the following side effects: cough. Vasotec dosage: .

6610877-7 | Hypoglycaemia
on Feb 12, 2010 Male patient from JAPAN , 70 years of age, was diagnosed with hypertension and was treated with Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: hypoglycaemia. Vasotec dosage: 1.25 Mg Qd Oral. During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ), NOVOLIN R (View Novolin R Review and Novolin R Label ). Patient was hospitalized.

6587737-3 | Angioedema
Patient was taking Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: angioedema on Feb 17, 2010 from UNITED STATES Additional patient health information: Male patient , 82 years of age, was diagnosed with hypertension and. Vasotec dosage: 10 Mg Q12h Po. During the same period patient was treated with COZAAR (50 Mg Qam Po) (View Cozaar Review and Cozaar Label ). Patient was hospitalized.

6571318-1 | Autonomic Nervous System Imbalance, Cerebral Infarction, Contusion, Fall, Haematocrit Decreased, Haematoma, Haemoglobin Decreased, Loss Of Consciousness, Neuropathy Peripheral
Adverse event was reported on Jan 25, 2010 by a Male patient taking Vasotec (View Usage) (Dosage: (df)) was diagnosed with acute myeloid leukaemia and. Location: UNITED STATES , weighting 145.5 lb, Patient had the following side effects: autonomic nervous system imbalance, cerebral infarction, contusion, fall (What is fall?), haematocrit decreased, haematoma, haemoglobin decreased, loss of consciousness, neuropathy peripheral. During the same period patient was treated with VELCADE ((1.3 Mg/m2, Cyclic), (1.0 Mg/m2, Cyclic)) (View Velcade Review and Velcade Label ), CYTARABINE ((100 Mg/m2, Cyclic), (2000 Mg/m2; Cyclic)) (View Cytarabine Review and Cytarabine Label ), ECOTRIN (NOT SPECIFIED) ((df)) (View Ecotrin (not Specified) Review and Ecotrin (not Specified) Label ), NEURONTIN ((df)) (View Neurontin Review and Neurontin Label ), PLAVIX ((df)) (View Plavix Review and Plavix Label ). Patient was hospitalized.

6552199-9 | Completed Suicide
on Jan 05, 2010 Female patient from UNITED STATES , 51 years of age, was treated with Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: completed suicide. Vasotec dosage: . During the same period patient was treated with BETABLOK (View Betablok Review and Betablok Label ), BUPROPION HYDROCHLORIDE (View Bupropion Hydrochloride Review and Bupropion Hydrochloride Label ), ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ), FLUOXETINE (View Fluoxetine Review and Fluoxetine Label ), ZESTRIL (View Zestril Review and Zestril Label ), ZOLPIDEM TARTRATE (View Zolpidem Tartrate Review and Zolpidem Tartrate Label ), FLEXERIL (View Flexeril Review and Flexeril Label ), GLIBENCLAMID (View Glibenclamid Review and Glibenclamid Label ).

6522864-8 | Balance Disorder, Hyperhidrosis, Hypotension, Incorrect Dose Administered
on Dec 09, 2009 Female patient from ITALY , 91 years of age, was treated with Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: balance disorder, hyperhidrosis, hypotension, incorrect dose administered. Vasotec dosage: . Patient was hospitalized.

6502041-7 | Agranulocytosis, Pancytopenia
Patient was taking Vasotec (View Usage). Patient had the following side effects: agranulocytosis, pancytopenia on Nov 26, 2009 from JAPAN Additional patient health information: Female patient , 80 years of age, . Vasotec dosage: (2.5 Mg Qd Oral).

6469113-7 | Liver Injury
Adverse event was reported on Nov 16, 2009 by a Female patient taking Vasotec (View Usage) (Dosage: (30 Mg Qd Oral)) . Location: SWEDEN , 74 years of age, After Vasotec was administered, patient had the following side effects: liver injury.

6466368-X | Blood Pressure Increased, Heart Rate Increased, Malaise
on Nov 17, 2009 Female patient from UNITED STATES , weighting 206.0 lb, was treated with Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, heart rate increased, malaise. Vasotec dosage: 10 Mg Qd. During the same period patient was treated with RED YEAST RICE (View Red Yeast Rice Review and Red Yeast Rice Label ), MULTIVITAMIN /00831701/ (View Multivitamin /00831701/ Review and Multivitamin /00831701/ Label ). Patient was hospitalized.

6458243-1 | Intracranial Pressure Increased
on Nov 18, 2009 Male patient from FRANCE , child 11 years of age, weighting 101.4 lb, was diagnosed with hypertension, bronchitis (What is bronchitis?) and was treated with Vasotec (View Usage). Patient had the following side effects: intracranial pressure increased. Vasotec dosage: . During the same period patient was treated with CALCIFEDIOL (View Calcifediol Review and Calcifediol Label ), COZAAR (View Cozaar Review and Cozaar Label ), AZITHROMYCIN (View Azithromycin Review and Azithromycin Label ), CALCIUM CARBONATE (View Calcium Carbonate Review and Calcium Carbonate Label ).

6452665-0 | Acute Prerenal Failure, Asthenia, Dehydration, Diarrhoea, Dizziness, Electrolyte Imbalance, Goitre, Hypotension
Patient was taking Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: acute prerenal failure, asthenia, dehydration, diarrhoea, dizziness (What is dizziness?), electrolyte imbalance, goitre, hypotension on Oct 29, 2009 from GERMANY Additional patient health information: Female patient , 71 years of age, was diagnosed with hypertension and. Vasotec dosage: . During the same period patient was treated with FUROSEMIDE ((40 Mg Qd Oral)) (View Furosemide Review and Furosemide Label ), METHYLDOPA ((250 Mg Bid Oral); (df Oral)) (View Methyldopa Review and Methyldopa Label ), MICARDIS ((80 Mg Qd Oral); (df Oral)) (View Micardis Review and Micardis Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), DIGITOXIN INJ (View Digitoxin Inj Review and Digitoxin Inj Label ). Patient was hospitalized.

6447339-6 | Balance Disorder, Hyperhidrosis, Hypotension, Incorrect Dose Administered
Adverse event was reported on Oct 30, 2009 by a Female patient taking Vasotec (View Usage) (Dosage: ) . Location: ITALY , 91 years of age, Patient experienced the following unwanted or unexpected effects: balance disorder, hyperhidrosis, hypotension, incorrect dose administered. Patient was hospitalized.

6431795-3 | Haemorrhage Subcutaneous
on Oct 04, 2009 Male patient from JAPAN , 84 years of age, was treated with Vasotec (View Usage). Patient had the following side effects: haemorrhage subcutaneous. Vasotec dosage: 2.5 Mg Qd Oral.

6416015-8 | Asthenia, Grand Mal Convulsion, Haemoglobin Decreased, Inappropriate Antidiuretic Hormone Secretion, Malaise
on Oct 08, 2009 Male patient from UNITED KINGDOM , 80 years of age, weighting 154.3 lb, was treated with Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: asthenia, grand mal convulsion, haemoglobin decreased, inappropriate antidiuretic hormone secretion, malaise. Vasotec dosage: (10 Mg Bid Oral) (10 Mg Bid Oral). During the same period patient was treated with ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ). Patient was hospitalized.

6404224-3 | Haemorrhage Subcutaneous
Patient was taking Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: haemorrhage subcutaneous on Sep 17, 2009 from JAPAN Additional patient health information: Male patient , 84 years of age, . Vasotec dosage: 2.5 Mg Qd Oral.

6403739-1 | Pancreatitis Acute, Polycythaemia
Adverse event was reported on Sep 15, 2009 by a Male patient taking Vasotec (View Usage) (Dosage: (20 Mg Qd Oral) ; (20 Mg Qd Oral)) was diagnosed with hypertension, hypercholesterolaemia and. Location: FRANCE , 73 years of age, Patient had the following side effects: pancreatitis acute, polycythaemia. During the same period patient was treated with FENOFIBRATE ((df Oral)) (View Fenofibrate Review and Fenofibrate Label ), ACETAMINOPHEN W/ CODEINE ((df Oral)) (View Acetaminophen W/ Codeine Review and Acetaminophen W/ Codeine Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), SAW PALMETTO (View Saw Palmetto Review and Saw Palmetto Label ). Patient was hospitalized.

6403054-6 | Asthenia, Bronchial Disorder, Chest Discomfort, Crying, Depression, Dizziness, Dyspnoea, Fatigue, Fear
on Oct 15, 2009 Female patient from UNITED STATES , 61 years of age, weighting 225.0 lb, was diagnosed with hypertension and was treated with Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: asthenia, bronchial disorder, chest discomfort, crying, depression (What is depression?), dizziness (What is dizziness?), dyspnoea, fatigue, fear. Vasotec dosage: 10mg 1 A Day. Patient was hospitalized and became disabled.

6371741-4 | Product Substitution Issue
on Sep 18, 2009 Female patient from UNITED STATES , weighting 173.0 lb, was treated with Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: product substitution issue. Vasotec dosage: 20mg Twice Daily, Prior To 2000 To Present.

6370444-X | Dyspnoea, Lip Swelling, Product Substitution Issue
Patient was taking Vasotec (View Usage). Patient had the following side effects: dyspnoea, lip swelling, product substitution issue on Sep 21, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 173.0 lb, . Vasotec dosage: 20mg Twice Daily Prior To 2000 To Present.

6346969-X | Abdominal Pain Upper
Adverse event was reported on Sep 09, 2009 by a Male patient taking Vasotec (View Usage) (Dosage: ? Once Iv Bolus Minutes) was diagnosed with hypertension and. Location: UNITED STATES , 52 years of age, weighting 170.0 lb, After Vasotec was administered, patient had the following side effects: abdominal pain upper.

6303804-3 | Blood Pressure Decreased, Bronchospasm, Cardio-respiratory Arrest, Electrocardiogram Qt Prolonged, Hyperkalaemia
on Aug 05, 2009 Male patient from FRANCE , 14 years of age, was diagnosed with hypertension, lung transplant (What is lung transplant?), prophylaxis against gastrointestinal ulcer and was treated with Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure decreased, bronchospasm, cardio-respiratory arrest, electrocardiogram qt prolonged, hyperkalaemia. Vasotec dosage: . During the same period patient was treated with COZAAR (View Cozaar Review and Cozaar Label ), TACROLIMUS (View Tacrolimus Review and Tacrolimus Label ), LEFLUNOMIDE (View Leflunomide Review and Leflunomide Label ), ACEBUTOLOL (View Acebutolol Review and Acebutolol Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), GUANFACINE HYDROCHLORIDE (View Guanfacine Hydrochloride Review and Guanfacine Hydrochloride Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

6256097-X | Blood Potassium Increased, Pancreatitis
on Jun 30, 2009 Male patient from UNITED STATES , 74 years of age, weighting 160.0 lb, was diagnosed with blood pressure (What is blood pressure?) and was treated with Vasotec (View Usage). Patient had the following side effects: blood potassium increased, pancreatitis. Vasotec dosage: 5 Mg Once/day Po. During the same period patient was treated with NORVASC (View Norvasc Review and Norvasc Label ), PEPCID INSULIN (View Pepcid Insulin Review and Pepcid Insulin Label ), GLUCOVANCE (View Glucovance Review and Glucovance Label ). Patient was hospitalized.

6232789-3 | Angioedema, Eosinophil Count Decreased, No Therapeutic Response
Patient was taking Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: angioedema, eosinophil count decreased, no therapeutic response on Jun 12, 2009 from UNITED STATES Additional patient health information: Male patient , 66 years of age, weighting 209.4 lb, was diagnosed with hypertension and. Vasotec dosage: 10mg Bid Po. During the same period patient was treated with COLACE (View Colace Review and Colace Label ), SENOKOT (View Senokot Review and Senokot Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ), VICODIN ES (View Vicodin Es Review and Vicodin Es Label ), FLEXERIL (View Flexeril Review and Flexeril Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ). Patient was hospitalized.

6231226-2 | Blood Creatinine Increased, Blood Urea Increased, Condition Aggravated, Creatinine Renal Clearance Decreased, Decreased Activity, Dilatation Ventricular, Dizziness, Dyspnoea
Adverse event was reported on May 26, 2009 by a Female patient taking Vasotec (View Usage) (Dosage: (2.5 Mg Qd Oral)) was diagnosed with hypertension, coronary artery disease (What is coronary artery disease?) and. Location: GERMANY , 71 years of age, Patient experienced the following unwanted or unexpected effects: blood creatinine increased, blood urea increased, condition aggravated, creatinine renal clearance decreased, decreased activity, dilatation ventricular, dizziness (What is dizziness?), dyspnoea. During the same period patient was treated with SPIRONOLACTONE ((25 Mg Qd Oral)) (View Spironolactone Review and Spironolactone Label ), ASPIRIN ((100 Mg Qd Oral)) (View Aspirin Review and Aspirin Label ), CANDESARTAN CILEXETIL ((8 Mg Qd Oral)) (View Candesartan Cilexetil Review and Candesartan Cilexetil Label ), BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), HYDROMORPHONE HCL (View Hydromorphone Hcl Review and Hydromorphone Hcl Label ), INSULIN ASPART (View Insulin Aspart Review and Insulin Aspart Label ), ISOSORBIDE DINITRATE (View Isosorbide Dinitrate Review and Isosorbide Dinitrate Label ). Patient was hospitalized.

6230686-0 | Inappropriate Antidiuretic Hormone Secretion
on May 29, 2009 Male patient from JAPAN , 62 years of age, was treated with Vasotec (View Usage). Patient had the following side effects: inappropriate antidiuretic hormone secretion. Vasotec dosage: (oral).

6206216-6 | Cough, Dyspnoea
on May 11, 2009 Male patient from UNITED STATES , 58 years of age, was treated with Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: cough, dyspnoea. Vasotec dosage: Df Oral.

6203651-7 | Atrial Fibrillation, Dysgraphia, Muscular Weakness, Product Substitution Issue, Pulmonary Fibrosis, Weight Decreased
Patient was taking Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: atrial fibrillation (What is atrial fibrillation?), dysgraphia, muscular weakness, product substitution issue, pulmonary fibrosis (What is pulmonary fibrosis?), weight decreased on May 05, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 125.0 lb, was diagnosed with cardiac failure and. Vasotec dosage: (5 Mg Bid), (df). During the same period patient was treated with ISOPTIN /00014301/ (View Isoptin /00014301/ Review and Isoptin /00014301/ Label ), PREVACID (View Prevacid Review and Prevacid Label ), INDOCIN /00003801/ (View Indocin /00003801/ Review and Indocin /00003801/ Label ), SYNTHROID (View Synthroid Review and Synthroid Label ). Patient was hospitalized and became disabled.

6191118-4 | Product Substitution Issue, Urticaria
Adverse event was reported on May 13, 2009 by a Female patient taking Vasotec (View Usage) (Dosage: Qd Po) was diagnosed with hypertension and. Location: UNITED STATES , weighting 154.0 lb, Patient had the following side effects: product substitution issue, urticaria.

6191116-0 | Product Substitution Issue
on May 13, 2009 Male patient from UNITED STATES , weighting 290.0 lb, was diagnosed with hypertension and was treated with Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: product substitution issue. Vasotec dosage: Qd Po.

6165990-8 | Angioedema, Cardio-respiratory Arrest, Stevens-johnson Syndrome, Toxic Epidermal Necrolysis, Urinary Tract Infection
on Apr 06, 2009 Female patient from UNITED STATES , 69 years of age, weighting 229.0 lb, was diagnosed with hypertension and was treated with Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: angioedema, cardio-respiratory arrest, stevens-johnson syndrome, toxic epidermal necrolysis, urinary tract infection (What is urinary tract infection?). Vasotec dosage: (2.5 Mg Bid Oral). During the same period patient was treated with ALLOPURINOL ((300 Mg Qd Oral)) (View Allopurinol Review and Allopurinol Label ), CLOPIDOGREL BISULFATE ((75 Mg Qd Oral)) (View Clopidogrel Bisulfate Review and Clopidogrel Bisulfate Label ), CEFEPIME ((1 G Qd Intravenous)) (View Cefepime Review and Cefepime Label ), VANCOMYCIN HCL ((intravenous)) (View Vancomycin Hcl Review and Vancomycin Hcl Label ), MINOXIDIL ((2.5 Mg Qd Oral)) (View Minoxidil Review and Minoxidil Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), ACETAMINOPHEN AND OXYCODONE HCL (View Acetaminophen And Oxycodone Hcl Review and Acetaminophen And Oxycodone Hcl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6153275-5 | Diarrhoea, Shock Hypoglycaemic
Patient was taking Vasotec (View Usage). Patient had the following side effects: diarrhoea, shock hypoglycaemic on Apr 01, 2009 from GERMANY Additional patient health information: Male patient , 83 years of age, was diagnosed with hypertension, type 2 diabetes mellitus and. Vasotec dosage: (10 Mg Bid Oral). During the same period patient was treated with INSULIN ACTRAPID /00646001/ (INSULIN ACTRAPID INSULIN HUMAN) (NOT SP ((22-10-20 Iu)) (View Insulin Actrapid /00646001/ (insulin Actrapid - Insulin Human) (not Sp Review and Insulin Actrapid /00646001/ (insulin Actrapid - Insulin Human) (not Sp Label ), PROTAPHANE /00646002/ (PROTAPHANE INSULIN HUMAN ISOPHANE) (NOT SPECI ((20 Iu Qd)) (View Protaphane /00646002/ (protaphane - Insulin Human Isophane) (not Speci Review and Protaphane /00646002/ (protaphane - Insulin Human Isophane) (not Speci Label ), ACETYLCYSTEINE (View Acetylcysteine Review and Acetylcysteine Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), DIGITOXIN TAB (View Digitoxin Tab Review and Digitoxin Tab Label ), NOVALGIN /00039501/ (View Novalgin /00039501/ Review and Novalgin /00039501/ Label ), BEROTEC (View Berotec Review and Berotec Label ), OXIS /00958002/ (View Oxis /00958002/ Review and Oxis /00958002/ Label ). Patient was hospitalized.

6143926-3 | Vomiting
Adverse event was reported on Mar 05, 2009 by a Male patient taking Vasotec (View Usage) (Dosage: (df Oral), (df Oral)) was diagnosed with cardiac failure congestive and. Location: SWEDEN , 67 years of age, After Vasotec was administered, patient had the following side effects: vomiting.

6106983-6 | Cough
on Mar 06, 2009 Female patient from UNITED STATES , weighting 178.0 lb, was diagnosed with hypertension and was treated with Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: cough. Vasotec dosage: Early To Mid 1980's 11-06 (tried Again).

6099939-3 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Rhabdomyolysis
on Feb 11, 2009 Female patient from BRAZIL , 68 years of age, was diagnosed with hypertension, hypercholesterolaemia and was treated with Vasotec (View Usage). Patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, rhabdomyolysis. Vasotec dosage: (df). During the same period patient was treated with SIMVASTATIN ((df)) (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized and became disabled.

5980239-4 | Cough, Dyspnoea, Throat Tightness
Patient was taking Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: cough, dyspnoea, throat tightness on Dec 02, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 200.0 lb, was diagnosed with hypertension and. Vasotec dosage: .

5968492-4 | Product Quality Issue, Pruritus, Rash
Adverse event was reported on Nov 21, 2008 by a Male patient taking Vasotec (View Usage) (Dosage: 1 Daily Po) was diagnosed with hypertension and. Location: UNITED STATES , weighting 165.0 lb, Patient experienced the following unwanted or unexpected effects: product quality issue, pruritus, rash (What is rash?).

5915935-8 | Dyspnoea
on Oct 06, 2008 Female patient from UNITED STATES , 56 years of age, weighting 454.2 lb, was diagnosed with hypertension, obesity (What is obesity?) and was treated with Vasotec (View Usage). Patient had the following side effects: dyspnoea. Vasotec dosage: . During the same period patient was treated with HYDRODIURIL (View Hydrodiuril Review and Hydrodiuril Label ), FELODIPINE (View Felodipine Review and Felodipine Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), TYLENOL (CAPLET) (View Tylenol (caplet) Review and Tylenol (caplet) Label ), COD LIVER OIL (View Cod Liver Oil Review and Cod Liver Oil Label ), GERITOL COMPLETE (View Geritol Complete Review and Geritol Complete Label ). Patient was hospitalized.

5908911-2 | Dyspnoea
on Sep 25, 2008 Female patient from UNITED STATES , 56 years of age, weighting 454.2 lb, was diagnosed with hypertension, obesity (What is obesity?) and was treated with Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: dyspnoea. Vasotec dosage: . During the same period patient was treated with HYDRODIURIL (View Hydrodiuril Review and Hydrodiuril Label ), FELODIPINE (View Felodipine Review and Felodipine Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), TYLENOL (CAPLET) (View Tylenol (caplet) Review and Tylenol (caplet) Label ), COD LIVER OIL (View Cod Liver Oil Review and Cod Liver Oil Label ), GERITOL COMPLETE (View Geritol Complete Review and Geritol Complete Label ). Patient was hospitalized.

5903344-7 | Hypertension, Hypotension, Malaise, Treatment Noncompliance
Patient was taking Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: hypertension, hypotension, malaise, treatment noncompliance on Sep 10, 2008 from UNITED STATES Additional patient health information: Female patient , 67 years of age, was diagnosed with arthritis (What is arthritis?), hypertension and. Vasotec dosage: (10 Mg At Bedtime). During the same period patient was treated with ROFECOXIB ((25 Mg Qd)) (View Rofecoxib Review and Rofecoxib Label ), VERAPAMIL HCL ((240 Mg Qd)) (View Verapamil Hcl Review and Verapamil Hcl Label ), NICOTINE ((df Transdermal)) (View Nicotine Review and Nicotine Label ), NEXIUM (View Nexium Review and Nexium Label ), AMBIEN (View Ambien Review and Ambien Label ), GLUCOVANCE (View Glucovance Review and Glucovance Label ), LOTREL (View Lotrel Review and Lotrel Label ), ZOCOR (View Zocor Review and Zocor Label ). Patient was hospitalized.

5866193-4 | Blood Pressure Decreased, Bronchospasm, Cardio-respiratory Arrest, Electrocardiogram Qt Prolonged, Hyperkalaemia
Adverse event was reported on Aug 25, 2008 by a Male patient taking Vasotec (View Usage) (Dosage: ) was diagnosed with hypertension, lung transplant (What is lung transplant?), prophylaxis against gastrointestinal ulcer and. Location: FRANCE , 14 years of age, Patient had the following side effects: blood pressure decreased, bronchospasm, cardio-respiratory arrest, electrocardiogram qt prolonged, hyperkalaemia. During the same period patient was treated with COZAAR (View Cozaar Review and Cozaar Label ), TACROLIMUS (View Tacrolimus Review and Tacrolimus Label ), LEFLUNOMIDE (View Leflunomide Review and Leflunomide Label ), ACEBUTOLOL (View Acebutolol Review and Acebutolol Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), GUANFACINE HYDROCHLORIDE (View Guanfacine Hydrochloride Review and Guanfacine Hydrochloride Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

5839836-9 | Ankle Fracture, Antiphospholipid Syndrome, Pulmonary Embolism
on Jul 31, 2008 Female patient from UNITED STATES , 52 years of age, was diagnosed with hypertension and was treated with Vasotec (View Usage). After Vasotec was administered, patient had the following side effects: ankle fracture, antiphospholipid syndrome, pulmonary embolism (What is pulmonary embolism?). Vasotec dosage: (40 Mg Qd). During the same period patient was treated with DYAZIDE (View Dyazide Review and Dyazide Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ). Patient was hospitalized.

5838377-2 | Anxiety, Back Pain, Chest Discomfort, Chest Pain, Hypotension, Neck Pain, Panic Reaction
on Jul 21, 2008 Male patient from UNITED STATES , 54 years of age, was diagnosed with back pain (What is back pain?), neck pain and was treated with Vasotec (View Usage). Patient experienced the following unwanted or unexpected effects: anxiety (What is anxiety?), back pain (What is back pain?), chest discomfort, chest pain (What is chest pain?), hypotension, neck pain, panic reaction. Vasotec dosage: 10 Mg Bid Oral, 5 Mg Bid Oral. During the same period patient was treated with CORTICOSTEROIDS (8 Epidural) (View Corticosteroids Review and Corticosteroids Label ), IMDUR (View Imdur Review and Imdur Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), CELEXA (View Celexa Review and Celexa Label ), LIPITOR (View Lipitor Review and Lipitor Label ), TENORMIN (View Tenormin Review and Tenormin Label ). Patient was hospitalized.

5823771-6 | Blood Pressure Decreased, Bronchospasm, Cardio-respiratory Arrest, Electrocardiogram Qt Prolonged, Hyperkalaemia
Patient was taking Vasotec (View Usage). Patient had the following side effects: blood pressure decreased, bronchospasm, cardio-respiratory arrest, electrocardiogram qt prolonged, hyperkalaemia on Jul 21, 2008 from FRANCE Additional patient health information: Male patient , 14 years of age, was diagnosed with hypertension, lung transplant (What is lung transplant?), prophylaxis against gastrointestinal ulcer and. Vasotec dosage: . During the same period patient was treated with COZAAR (View Cozaar Review and Cozaar Label ), TACROLIMUS (View Tacrolimus Review and Tacrolimus Label ), LEFLUNOMIDE (View Leflunomide Review and Leflunomide Label ), ACEBUTOLOL (View Acebutolol Review and Acebutolol Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), GUANFACINE HYDROCHLORIDE (View Guanfacine Hydrochloride Review and Guanfacine Hydrochloride Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

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To find out about documented side effects or safety concerns read either the drug label or the drug's package insert. You may also want to speak with your pharmacist or healthcare provider. All medicines have benefits and risks. The risks are the chances that something unwanted or unexpected could happen to you when you use them. You can protect yourself by searching summaries of recent safety alerts, adverse reports. Sometimes there are risks that only come to light after a medical product gets on the market and is used in a larger number of patients, for a longer period of time, and in patients whose health characteristics are different from those of the patients studied before approval.

Be aware of the following potential Vasotec risks to be aware of: 1. Watch for any Serious adverse events, such as life-threatening situation, which can require an admission to hospital or longer-than-expected hospital stay, permanent disability, birth defect, miscarriage, stillbirth, or birth with serious disease requires medical care to prevent permanent damage
2. Any potential Vasotec quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Vasotec use error: mixing up products with similar drug names or packaging, taking wrong dose of a drug because of confusing dosing instructions on label
4. When applicable, Problems with different manufacturer of same medicine: not getting same results from a generic drug as a brand name drug, or from another generic

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Vasotec Reactions
Amnesia
Angioedema
Angioneurotic Oedema
Asthenia
Blood Pressure Decreased
Blood Pressure Inadequately Controlled
Blood Pressure Increased
Cerebrovascular Accident
Chest PainWhat is Chest pain?
Condition Aggravated
Cough
DepressionWhat is Depression?
Diarrhoea
DizzinessWhat is Dizziness?
Dyspnoea
Feeling Abnormal
Flushing
HeadacheWhat is Headache?
Heart Rate Increased
Hyperkalaemia
Hypersensitivity
Hypertension
Hypotension
Malaise
NauseaWhat is Nausea?
Palpitations
Product Substitution Issue
RashWhat is Rash?
Renal Failure
Tremor
Vasotec Side Effects Notice - The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. PatientsVille.com does not provide medical advice, diagnosis or treatment. The information regarding Vasotec adverse reports, reviews and polls contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments. Thank you for visiting Patientsville.com!