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Summary

FDA Adverse Reports: 187. View All

Accupril FDA safety alerts: No

Reported deaths: 8

Reported hospitalizations: 63

Accupril Dosage, Warnings, Usage.

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1Glaucoma
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Severe Urticaria including swelling of eyes, lips

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Often additional risks of using a medication, such as Accupril, 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 Accupril users, Learn more about unwanted side effects & find ways to reduce them. Browse Accupril Adverse Reports reported to FDA and participate in Accupril discussion, find alternative treatments and find ways to avoid or reduce risks associated with using Accupril. 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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Accupril Adverse Effect Reports (FDA)

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Showing 1-50 of 187  Next Page  >

7013033-6 |
on Sep 17, 2010 Female patient from PERU , 81 years of age, was diagnosed with hypertension and was treated with Accupril (View Usage). . Accupril dosage: 20 Mg, 1x/day.

6944517-4 |
Patient was taking Accupril (View Usage). on Aug 19, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 399.0 lb, was diagnosed with hypertension, pain (What is pain?) and. Accupril dosage: 10 Mg, 1x/day. During the same period patient was treated with NAPROSYN (250 Mg, 2x/day) (View Naprosyn Review and Naprosyn Label ), LASIX (40 Mg, 1x/day) (View Lasix Review and Lasix Label ), POTASSIUM (10 Mg, 1x/day) (View Potassium Review and Potassium Label ).

6916870-9 | Blood Pressure Inadequately Controlled, Chromaturia, Weight Increased
Adverse event was reported on May 19, 2008 by a Female patient taking Accupril (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , weighting 150.4 lb, After Accupril was administered, patient had the following side effects: blood pressure inadequately controlled, chromaturia, weight increased. During the same period patient was treated with CALCIUM CHANNEL BLOCKERS (View Calcium Channel Blockers Review and Calcium Channel Blockers Label ), LIPITOR (View Lipitor Review and Lipitor Label ).

6906656-3 | Cardiac Disorder
on Jul 26, 2010 Female patient from COLOMBIA , 69 years of age, was diagnosed with hypertension, dyspepsia and was treated with Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac disorder. Accupril dosage: 20 Mg, 2x/day. During the same period patient was treated with BETALOC (50 Mg, 1x/day) (View Betaloc Review and Betaloc Label ), ALSUCRAL (Unk) (View Alsucral Review and Alsucral Label ).


6886434-4 | Insomnia
on Jun 16, 2009 Male patient from UNITED STATES , weighting 220.0 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). Patient had the following side effects: insomnia. Accupril dosage: 20 Mg, 1x/day. During the same period patient was treated with ASPIRINE (Unk) (View Aspirine Review and Aspirine Label ).

6886375-2 | Cough
Patient was taking Accupril (View Usage). After Accupril was administered, patient had the following side effects: cough on Apr 17, 2009 from UNITED STATES Additional patient health information: Male patient , 54 years of age, . Accupril dosage: Unk.

6886227-8 | Abdominal Pain, Coeliac Disease, Diarrhoea, Nausea
Adverse event was reported on Feb 29, 2008 by a Female patient taking Accupril (View Usage) (Dosage: ) was diagnosed with hypertension, coronary artery disease (What is coronary artery disease?), chronic obstructive pulmonary disease, thyroid disorder and. Location: UNITED STATES , weighting 175.0 lb, Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), coeliac disease, diarrhoea, nausea (What is nausea?). During the same period patient was treated with QUINAPRIL (View Quinapril Review and Quinapril Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), PLAVIX (View Plavix Review and Plavix Label ), SYNTHROID (View Synthroid Review and Synthroid Label ).

6886008-5 | Alopecia
on Jun 25, 2008 Female patient from UNITED STATES , weighting 160.0 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). Patient had the following side effects: alopecia. Accupril dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ).

6885964-9 | Dysphagia, Retching, Vomiting
on Jun 05, 2008 Female patient from UNITED STATES , weighting 102.3 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). After Accupril was administered, patient had the following side effects: dysphagia, retching, vomiting. Accupril dosage: . During the same period patient was treated with NIASPAN (View Niaspan Review and Niaspan Label ), ZOCOR (View Zocor Review and Zocor Label ).

6885755-9 | Blood Pressure Inadequately Controlled
Patient was taking Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure inadequately controlled on Feb 26, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 294.1 lb, was diagnosed with hypertension, blood glucose abnormal and. Accupril dosage: 20 Mg, 2x/day. During the same period patient was treated with METFORMIN (Unk) (View Metformin Review and Metformin Label ), STARLIX (Unk) (View Starlix Review and Starlix Label ), ACTOS (Unk) (View Actos Review and Actos Label ).

6885626-8 | Pruritus, Rash
Adverse event was reported on Aug 22, 2008 by a Female patient taking Accupril (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , weighting 300.7 lb, Patient had the following side effects: pruritus, rash (What is rash?). During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ), METFORMIN HYDROCHLORIDE (View Metformin Hydrochloride Review and Metformin Hydrochloride Label ), PLAVIX (View Plavix Review and Plavix Label ), SITAGLIPTIN (View Sitagliptin Review and Sitagliptin Label ), COREG (View Coreg Review and Coreg Label ).

6885603-7 | Skin Fissures
on Mar 07, 2008 Male patient from UNITED STATES , weighting 215.4 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). After Accupril was administered, patient had the following side effects: skin fissures. Accupril dosage: . During the same period patient was treated with LOVASTATIN (View Lovastatin Review and Lovastatin Label ).

6885003-X | Blood Pressure Increased, Dyspnoea
on Oct 18, 2007 Male patient from UNITED STATES , weighting 240.5 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, dyspnoea. Accupril dosage: Daily. During the same period patient was treated with NEXIUM (View Nexium Review and Nexium Label ).

6884910-1 | Hypertension
Patient was taking Accupril (View Usage). Patient had the following side effects: hypertension on Oct 09, 2007 from UNITED STATES Additional patient health information: Female patient , weighting 215.5 lb, was diagnosed with hypertension and. Accupril dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), FOSAMAX (View Fosamax Review and Fosamax Label ).

6884820-X | Aphonia, Fatigue, Hypersensitivity, Oropharyngeal Pain, Rash
Adverse event was reported on Sep 21, 2007 by a Male patient taking Accupril (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , weighting 190.4 lb, After Accupril was administered, patient had the following side effects: aphonia, fatigue, hypersensitivity, oropharyngeal pain, rash (What is rash?). During the same period patient was treated with PRILOSEC (View Prilosec Review and Prilosec Label ).

6884742-4 | Somnolence
on Aug 21, 2007 Male patient from UNITED STATES , weighting 196.2 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: somnolence. Accupril dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ).

6884695-9 | Arthralgia, Arthritis, Cystitis
on Jul 26, 2007 Female patient from UNITED STATES , 80 years of age, weighting 125.7 lb, was diagnosed with blood pressure (What is blood pressure?) and was treated with Accupril (View Usage). Patient had the following side effects: arthralgia, arthritis (What is arthritis?), cystitis. Accupril dosage: .

6884621-2 | Angioedema
Patient was taking Accupril (View Usage). After Accupril was administered, patient had the following side effects: angioedema on Aug 14, 2007 from UNITED STATES Additional patient health information: Female patient , weighting 140.3 lb, was diagnosed with hypertension and. Accupril dosage: .

6884205-6 | Blood Pressure Inadequately Controlled
Adverse event was reported on Oct 23, 2003 by a Female patient taking Accupril (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , 70 years of age, weighting 180.0 lb, Patient experienced the following unwanted or unexpected effects: blood pressure inadequately controlled. During the same period patient was treated with NORVASC (View Norvasc Review and Norvasc Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

6882514-8 | Blood Pressure Inadequately Controlled, Diarrhoea, Paraesthesia, Tinnitus
on Nov 03, 2009 Male patient from UNITED STATES , weighting 160.1 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). Patient had the following side effects: blood pressure inadequately controlled, diarrhoea, paraesthesia, tinnitus (What is tinnitus?). Accupril dosage: . During the same period patient was treated with QUINAPRIL HCL (View Quinapril Hcl Review and Quinapril Hcl Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), LIPITOR (View Lipitor Review and Lipitor Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), AMBIEN (View Ambien Review and Ambien Label ). Patient was hospitalized.

6580560-5 | Hypertension, Myocardial Infarction
on Feb 04, 2010 Male patient from UNITED STATES , weighting 82.01 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). After Accupril was administered, patient had the following side effects: hypertension, myocardial infarction. Accupril dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), GLUCOPHAGE (View Glucophage Review and Glucophage Label ), ALLEGRA (View Allegra Review and Allegra Label ), NASACORT (View Nasacort Review and Nasacort Label ), SYMBICORT (View Symbicort Review and Symbicort Label ), MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ), NIASPAN (View Niaspan Review and Niaspan Label ), PLAVIX (View Plavix Review and Plavix Label ).

6554626-X | Heart Valve Replacement, Multiple Sclerosis, Walking Disability
Patient was taking Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: heart valve replacement, multiple sclerosis (What is multiple sclerosis?), walking disability on Jan 19, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 175.0 lb, was diagnosed with hypertension, heart valve replacement and. Accupril dosage: 40 Mg, Daily. During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized and became disabled.

6536592-6 | Heart Valve Replacement, Multiple Sclerosis, Walking Disability
Adverse event was reported on Jan 05, 2010 by a Male patient taking Accupril (View Usage) (Dosage: 40 Mg, Daily) was diagnosed with hypertension, heart valve replacement and. Location: UNITED STATES , weighting 175.0 lb, Patient had the following side effects: heart valve replacement, multiple sclerosis (What is multiple sclerosis?), walking disability. During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized and became disabled.

6524918-9 | Heart Valve Replacement, Multiple Sclerosis, Walking Disability
on Dec 22, 2009 Male patient from UNITED STATES , weighting 175.0 lb, was diagnosed with hypertension, heart valve replacement and was treated with Accupril (View Usage). After Accupril was administered, patient had the following side effects: heart valve replacement, multiple sclerosis (What is multiple sclerosis?), walking disability. Accupril dosage: 40 Mg, Daily. During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized and became disabled.

6456172-0 | Blood Cholesterol Increased, Blood Glucose Decreased, Constipation, Diabetes Mellitus, Hypersensitivity, Hypotension
on Nov 16, 2009 Male patient from UNITED STATES , weighting 295.0 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: blood cholesterol increased, blood glucose decreased, constipation (What is constipation?), diabetes mellitus, hypersensitivity, hypotension. Accupril dosage: 20 Mg, 1x/day. During the same period patient was treated with NORVASC (View Norvasc Review and Norvasc Label ), GABAPENTIN (Frequency: 2x/day,) (View Gabapentin Review and Gabapentin Label ), ZOLOFT (100 Mg, Daily) (View Zoloft Review and Zoloft Label ), PROTONIX (View Protonix Review and Protonix Label ), TYLENOL (CAPLET) (Frequency: As Needed,) (View Tylenol (caplet) Review and Tylenol (caplet) Label ), SALICYLIC ACID (View Salicylic Acid Review and Salicylic Acid Label ), RISPERDAL (View Risperdal Review and Risperdal Label ), BENAZEPRIL HYDROCHLORIDE (View Benazepril Hydrochloride Review and Benazepril Hydrochloride Label ).

6384259-X | Conjunctivitis, Fatigue, Traumatic Haematoma, Vascular Occlusion
Patient was taking Accupril (View Usage). Patient had the following side effects: conjunctivitis, fatigue, traumatic haematoma, vascular occlusion on Sep 20, 2009 from UNITED STATES Additional patient health information: Male patient , weighting 169.8 lb, was diagnosed with cardiac disorder, stent placement, blood cholesterol and. Accupril dosage: 40 Mg, 1x/day. During the same period patient was treated with PLAVIX (75 Mg, 1x/day) (View Plavix Review and Plavix Label ), COREG (60 Mg, 1x/day) (View Coreg Review and Coreg Label ), LIPITOR (50 Mg, 1x/day) (View Lipitor Review and Lipitor Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ).

6376512-0 | Abdominal Pain Upper, Blood Pressure Inadequately Controlled, Breast Cancer, Cardiac Disorder, Hypersensitivity, Malaise, Pharyngitis
Adverse event was reported on Sep 15, 2009 by a Female patient taking Accupril (View Usage) (Dosage: 10 Mg, 1x/day Every Day) was diagnosed with hypertension and. Location: UNITED STATES , weighting 164.9 lb, After Accupril was administered, patient had the following side effects: abdominal pain upper, blood pressure inadequately controlled, breast cancer (What is breast cancer?), cardiac disorder, hypersensitivity, malaise, pharyngitis.

6315987-X | Fatigue, Product Substitution Issue
on Aug 19, 2009 Female patient from UNITED STATES , weighting 145.0 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: fatigue, product substitution issue. Accupril dosage: 1 Qd Po.

6309821-1 | Conjunctivitis, Fatigue, Traumatic Haematoma, Vascular Occlusion
on Aug 06, 2009 Male patient from UNITED STATES , weighting 169.8 lb, was diagnosed with cardiac disorder, stent placement, blood cholesterol and was treated with Accupril (View Usage). Patient had the following side effects: conjunctivitis, fatigue, traumatic haematoma, vascular occlusion. Accupril dosage: 40 Mg, 1x/day. During the same period patient was treated with PLAVIX (75 Mg, 1x/day) (View Plavix Review and Plavix Label ), COREG (60 Mg, 1x/day) (View Coreg Review and Coreg Label ), LIPITOR (50 Mg, 1x/day) (View Lipitor Review and Lipitor Label ), ACETYLSALICYLIC ACID (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ).

6304036-5 | Abdominal Pain Upper, Blood Pressure Inadequately Controlled, Breast Cancer, Cardiac Disorder, Hypersensitivity, Malaise, Pharyngitis
Patient was taking Accupril (View Usage). After Accupril was administered, patient had the following side effects: abdominal pain upper, blood pressure inadequately controlled, breast cancer (What is breast cancer?), cardiac disorder, hypersensitivity, malaise, pharyngitis on Jul 31, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 164.9 lb, was diagnosed with hypertension and. Accupril dosage: 10 Mg, 1x/day Every Day.

6294346-2 | Back Pain, Blood Pressure Inadequately Controlled, Blood Pressure Increased, Breast Cancer, Panic Attack
Adverse event was reported on Aug 03, 2009 by a Female patient taking Accupril (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , weighting 150.0 lb, Patient experienced the following unwanted or unexpected effects: back pain (What is back pain?), blood pressure inadequately controlled, blood pressure increased, breast cancer (What is breast cancer?), panic attack. During the same period patient was treated with ACCURETIC (View Accuretic Review and Accuretic Label ), NORVASC (View Norvasc Review and Norvasc Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ). Patient was hospitalized.

6247192-X | Back Pain, Blood Pressure Inadequately Controlled, Blood Pressure Increased, Breast Cancer, Panic Attack
on Jun 18, 2009 Female patient from UNITED STATES , 49 years of age, was diagnosed with hypertension and was treated with Accupril (View Usage). Patient had the following side effects: back pain (What is back pain?), blood pressure inadequately controlled, blood pressure increased, breast cancer (What is breast cancer?), panic attack. Accupril dosage: . During the same period patient was treated with ACCURETIC (View Accuretic Review and Accuretic Label ), NORVASC (View Norvasc Review and Norvasc Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ). Patient was hospitalized.

6199454-2 |
on May 15, 2009 Female patient from PERU , 60 years of age, was diagnosed with hypertension and was treated with Accupril (View Usage). . Accupril dosage: 40 Mg, 1x/day.

6180804-8 | Bronchitis, Hypokalaemia, Hyponatraemia, Laryngitis, Sinus Disorder
Patient was taking Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: bronchitis (What is bronchitis?), hypokalaemia, hyponatraemia, laryngitis, sinus disorder on Apr 28, 2009 from UNITED STATES Additional patient health information: Female patient , weighting 154.0 lb, was diagnosed with hypertension and. Accupril dosage: . During the same period patient was treated with AMLODIPINE BESYLATE (5 Mg, 1x/day) (View Amlodipine Besylate Review and Amlodipine Besylate Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), SYNTHROID (Unk) (View Synthroid Review and Synthroid Label ), WELCHOL (View Welchol Review and Welchol Label ), GEMFIBROZIL (View Gemfibrozil Review and Gemfibrozil Label ), MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ), CALCIUM WITH VITAMIN D (View Calcium With Vitamin D Review and Calcium With Vitamin D Label ). Patient was hospitalized.

6086872-6 | Blood Pressure Increased, Creatinine Renal Clearance Decreased, Glaucoma
Adverse event was reported on Feb 12, 2009 by a Female patient taking Accupril (View Usage) (Dosage: 10 Mg, 1x/day) was diagnosed with hypertension and. Location: UNITED STATES , weighting 149.9 lb, Patient had the following side effects: blood pressure increased, creatinine renal clearance decreased, glaucoma (What is glaucoma?). During the same period patient was treated with ACETYLSALICYLIC ACID (Unk) (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ).

6063224-6 | Blood Cholesterol Increased, Fatigue, Feeling Abnormal, Irritability
on Jan 25, 2009 Female patient from UNITED STATES , weighting 150.0 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). After Accupril was administered, patient had the following side effects: blood cholesterol increased, fatigue, feeling abnormal, irritability. Accupril dosage: 5 Mg, 2x/day.

6044543-6 | Blood Pressure Decreased, Chest Pain, Diabetes Mellitus, Dizziness, Headache, Skin Burning Sensation, Sunburn, Vascular Injury, Vision Blurred
on Aug 13, 2008 Female patient from CANADA , 74 years of age, was diagnosed with blood pressure increased, cerebrovascular accident and was treated with Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure decreased, chest pain (What is chest pain?), diabetes mellitus, dizziness (What is dizziness?), headache (What is headache?), skin burning sensation, sunburn, vascular injury, vision blurred. Accupril dosage: . During the same period patient was treated with NORVASC (View Norvasc Review and Norvasc Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), PLAVIX (View Plavix Review and Plavix Label ), PRAVACHOL (Unk) (View Pravachol Review and Pravachol Label ).

6013409-X | Blood Cholesterol Increased, Fatigue, Feeling Abnormal, Irritability
Patient was taking Accupril (View Usage). Patient had the following side effects: blood cholesterol increased, fatigue, feeling abnormal, irritability on Dec 10, 2008 from UNITED STATES Additional patient health information: Female patient , weighting 150.0 lb, was diagnosed with hypertension and. Accupril dosage: 5 Mg, 2x/day.

5928447-2 | Dizziness, Fatigue, Loss Of Consciousness, Somnolence, Vitamin B12 Deficiency
Adverse event was reported on Oct 17, 2008 by a Male patient taking Accupril (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , weighting 189.4 lb, After Accupril was administered, patient had the following side effects: dizziness (What is dizziness?), fatigue, loss of consciousness, somnolence, vitamin b12 deficiency. During the same period patient was treated with FOLIC ACID (View Folic Acid Review and Folic Acid Label ), CYANOCOBALAMIN (View Cyanocobalamin Review and Cyanocobalamin Label ), GLUCOSAMINE (View Glucosamine Review and Glucosamine Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ).

5874453-6 | Bradycardia, Syncope
on Aug 27, 2008 Male patient from UNITED STATES , 63 years of age, weighting 207.2 lb, was diagnosed with renal cell carcinoma and was treated with Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, syncope. Accupril dosage: . During the same period patient was treated with OMACOR (View Omacor Review and Omacor Label ), COREG (View Coreg Review and Coreg Label ), HUMALOG (Text:25 Mg In Am; 25 Mg In Pm (50/50)) (View Humalog Review and Humalog Label ), HYDRALAZINE HYDROCHLORIDE (View Hydralazine Hydrochloride Review and Hydralazine Hydrochloride Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), NOVOLOG (Text:100 Units/ml-freq:tid) (View Novolog Review and Novolog Label ), PRAVACHOL (View Pravachol Review and Pravachol Label ). Patient was hospitalized.

5851887-7 | Hypertension, Myocardial Infarction
on Aug 13, 2008 Male patient from UNITED STATES , weighting 82.01 lb, was diagnosed with hypertension and was treated with Accupril (View Usage). Patient had the following side effects: hypertension, myocardial infarction. Accupril dosage: . During the same period patient was treated with GLUCOPHAGE (View Glucophage Review and Glucophage Label ), ALLEGRA (View Allegra Review and Allegra Label ), NASACORT (View Nasacort Review and Nasacort Label ), SYMBICORT (View Symbicort Review and Symbicort Label ), MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ), NIASPAN (View Niaspan Review and Niaspan Label ), LIPITOR (View Lipitor Review and Lipitor Label ), PLAVIX (View Plavix Review and Plavix Label ).

5846106-1 | Hypertension, Myocardial Infarction
Patient was taking Accupril (View Usage). After Accupril was administered, patient had the following side effects: hypertension, myocardial infarction on Aug 05, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 82.01 lb, was diagnosed with hypertension and. Accupril dosage: . During the same period patient was treated with GLUCOPHAGE (View Glucophage Review and Glucophage Label ), ALLEGRA (View Allegra Review and Allegra Label ), NASACORT (View Nasacort Review and Nasacort Label ), SYMBICORT (View Symbicort Review and Symbicort Label ), MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ), NIASPAN (View Niaspan Review and Niaspan Label ), LIPITOR (View Lipitor Review and Lipitor Label ), PLAVIX (View Plavix Review and Plavix Label ).

5846014-6 | Blood Pressure Increased, Cerebrovascular Accident, Headache, Peripheral Vascular Disorder
Adverse event was reported on Aug 05, 2008 by a Female patient taking Accupril (View Usage) (Dosage: Daily Dose:20mg-freq:daily) was diagnosed with blood pressure (What is blood pressure?) and. Location: UNITED STATES , weighting 179.9 lb, Patient experienced the following unwanted or unexpected effects: blood pressure increased, cerebrovascular accident, headache (What is headache?), peripheral vascular disorder. During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PRAVACHOL (View Pravachol Review and Pravachol Label ), MESCOLOR (View Mescolor Review and Mescolor Label ).

5844650-4 | No Adverse Event
on Aug 05, 2008 Female patient from UNITED STATES , weighting 115.2 lb, was diagnosed with hypertension, cardiac disorder and was treated with Accupril (View Usage). Patient had the following side effects: no adverse event. Accupril dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ).

5760476-4 | Blood Pressure Inadequately Controlled, Renal Disorder
on May 29, 2008 Female patient from UNITED STATES , weighting 115.2 lb, was diagnosed with hypertension, cardiac disorder and was treated with Accupril (View Usage). After Accupril was administered, patient had the following side effects: blood pressure inadequately controlled, renal disorder. Accupril dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ).

5751386-7 | Hypersensitivity, Myalgia, Nodule, Visual Disturbance
Patient was taking Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: hypersensitivity, myalgia, nodule, visual disturbance on May 20, 2008 from BRAZIL Additional patient health information: Female patient , 66 years of age, was diagnosed with hypertension and. Accupril dosage: . Patient was hospitalized.

5592902-8 | Cognitive Disorder, Dementia Alzheimer's Type
Adverse event was reported on Jan 14, 2008 by a Male patient taking Accupril (View Usage) (Dosage: ) was diagnosed with blood pressure increased and. Location: UNITED STATES , weighting 190.0 lb, Patient had the following side effects: cognitive disorder, dementia alzheimer's type. During the same period patient was treated with STEROID (View Steroid Review and Steroid Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ).

5502366-8 | Arthritis, Joint Effusion, Joint Sprain, Oesophageal Spasm
on Oct 22, 2007 Female patient from UNITED STATES , 86 years of age, was diagnosed with hypertension and was treated with Accupril (View Usage). After Accupril was administered, patient had the following side effects: arthritis (What is arthritis?), joint effusion, joint sprain, oesophageal spasm. Accupril dosage: . During the same period patient was treated with CATAPRES (View Catapres Review and Catapres Label ), DYNACIRC (View Dynacirc Review and Dynacirc Label ), AMILORIDE HYDROCHLORIDE (View Amiloride Hydrochloride Review and Amiloride Hydrochloride Label ), LASIX (View Lasix Review and Lasix Label ).

5470154-7 | Blood Amylase Increased, Blood Bilirubin Increased, Nasal Disorder, Pancreatic Cyst, Pigmentation Disorder
on Sep 18, 2007 Female patient from UNITED STATES , weighting 102.2 lb, was diagnosed with hypertension, osteoporosis (What is osteoporosis?) and was treated with Accupril (View Usage). Patient experienced the following unwanted or unexpected effects: blood amylase increased, blood bilirubin increased, nasal disorder, pancreatic cyst, pigmentation disorder. Accupril dosage: Daily Dose:5mg-freq:daily. During the same period patient was treated with MIACALCIN (View Miacalcin Review and Miacalcin Label ).

5422170-9 | Lip Swelling
Patient was taking Accupril (View Usage). Patient had the following side effects: lip swelling on Aug 21, 2007 from UNITED STATES Additional patient health information: Male patient , weighting 151.8 lb, was diagnosed with hypertension, pain (What is pain?) and. Accupril dosage: 40mg Qd Po. During the same period patient was treated with NAPROSYN (375 Mg Bid Prn Po) (View Naprosyn Review and Naprosyn Label ).

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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 Accupril 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 Accupril quality problem: suspected counterfeit product, potentially contaminated product indicated by suspicious odor or unusual color, inaccurate or unreadable product labeling
3. Potential Accupril 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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Accupril Reactions
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Accupril 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 Accupril 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!