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Quinapril Adverse Events Reported to the FDA Over Time

How are Quinapril adverse event reports trending over time?

This graph shows volume of adverse events submitted to the FDA by quarter for Quinapril, as well as related generic and/or brandname drugs containing the same primary active ingredients. Adverse events are counted if Quinapril is flagged as the suspect drug causing the adverse event.

Most Common Quinapril Adverse Events Reported to the FDA

What are the most common Quinapril adverse events reported to the FDA?

Drug Ineffective
52 (1.83%)
Dizziness
48 (1.69%)
Dyspnoea
45 (1.58%)
Headache
40 (1.41%)
Diarrhoea
35 (1.23%)
Blood Pressure Increased
34 (1.2%)
Nausea
33 (1.16%)
Hypertensive Emergency
32 (1.12%)
Cough
30 (1.05%)
Chest Pain
28 (.98%)
Hypertension
28 (.98%)
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Oedema Peripheral
28 (.98%)
Hypotension
27 (.95%)
Malaise
27 (.95%)
Blood Pressure Inadequately Control...
26 (.91%)
Hyperkalaemia
26 (.91%)
Renal Failure Acute
25 (.88%)
Death
23 (.81%)
Hypersensitivity
23 (.81%)
Blood Glucose Increased
22 (.77%)
Drug Interaction
22 (.77%)
Asthenia
21 (.74%)
Confusional State
21 (.74%)
Hyperhidrosis
20 (.7%)
Swollen Tongue
19 (.67%)
Angioedema
18 (.63%)
Cardiac Arrest
18 (.63%)
Erythema
18 (.63%)
Gait Disturbance
17 (.6%)
Myalgia
17 (.6%)
Abdominal Discomfort
16 (.56%)
Completed Suicide
16 (.56%)
Convulsion
16 (.56%)
Feeling Abnormal
16 (.56%)
Pancytopenia
16 (.56%)
Tachycardia
16 (.56%)
Anaemia
15 (.53%)
Somnolence
15 (.53%)
Blood Creatinine Increased
14 (.49%)
Condition Aggravated
14 (.49%)
Dehydration
14 (.49%)
Lip Swelling
14 (.49%)
Pain
14 (.49%)
Vomiting
14 (.49%)
Red Blood Cell Count Decreased
13 (.46%)
Respiratory Arrest
13 (.46%)
Agitation
12 (.42%)
Eye Irritation
12 (.42%)
Fall
12 (.42%)
Flushing
12 (.42%)
Haematocrit Decreased
12 (.42%)
Haemoglobin Decreased
12 (.42%)
Orthostatic Hypotension
12 (.42%)
Overdose
12 (.42%)
Pruritus
12 (.42%)
Rhabdomyolysis
12 (.42%)
Swelling Face
12 (.42%)
Therapeutic Response Unexpected Wit...
12 (.42%)
Blood Pressure Decreased
11 (.39%)
Cardiotoxicity
11 (.39%)
Dysuria
11 (.39%)
Loss Of Consciousness
11 (.39%)
Pharyngeal Oedema
11 (.39%)
Rash Erythematous
11 (.39%)
Syncope
11 (.39%)
Weight Decreased
11 (.39%)
Atrial Fibrillation
10 (.35%)
Atrioventricular Block Complete
10 (.35%)
Cerebrovascular Accident
10 (.35%)
Electrocardiogram Qrs Complex Prolo...
10 (.35%)
Fatigue
10 (.35%)
Multiple Drug Overdose
10 (.35%)
Renal Failure Chronic
10 (.35%)
Urine Flow Decreased
10 (.35%)
Weight Increased
10 (.35%)
Bradycardia
9 (.32%)
Cardiac Murmur
9 (.32%)
Cardiogenic Shock
9 (.32%)
Drug Hypersensitivity
9 (.32%)
Medication Residue
9 (.32%)
Mydriasis
9 (.32%)
Pain In Extremity
9 (.32%)
Rash
9 (.32%)
Tinnitus
9 (.32%)
Blood Magnesium Increased
8 (.28%)
Blood Urea Increased
8 (.28%)
Coronary Arterial Stent Insertion
8 (.28%)
Decreased Appetite
8 (.28%)
Drug Effect Decreased
8 (.28%)
Dysgeusia
8 (.28%)
High Density Lipoprotein Decreased
8 (.28%)
Hypokalaemia
8 (.28%)
Hyponatraemia
8 (.28%)
Low Density Lipoprotein Increased
8 (.28%)
Poisoning Deliberate
8 (.28%)
Red Blood Cell Count Increased
8 (.28%)
Subileus
8 (.28%)
Total Cholesterol/hdl Ratio Decreas...
8 (.28%)
Bladder Discomfort
7 (.25%)
Blood Cholesterol Increased
7 (.25%)
Blood Uric Acid Increased
7 (.25%)

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This graph shows the top adverse events submitted to the FDA for Quinapril, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Quinapril is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Adverse Event Categories for Quinapril

What are the most common Quinapril adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Quinapril, as well as related generic and/or brandname drugs containing the same primary active ingredients, from Q1 2004 to Q3 2012. Adverse events are counted if Quinapril is flagged as a suspect drug causing the adverse event. For each adverse event listed, percent (%) represents percentage of the adverse event to all adverse events reported for the drug. Percent does not represent a rate related to drug utilization.

Common Uses of Quinapril According to Those Reporting Adverse Events

Why are people taking Quinapril, according to those reporting adverse events to the FDA?

Hypertension
874
Drug Use For Unknown Indication
206
Product Used For Unknown Indication
183
Blood Pressure
96
Ill-defined Disorder
37
Blood Pressure Abnormal
35
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Cardiac Disorder
22
Essential Hypertension
20
Coronary Artery Disease
18
Blood Pressure Increased
14
Cardiac Failure
11
Cardiac Failure Congestive
8
Prophylaxis
7
Cardiomyopathy
6
Myocardial Infarction
6
Myocardial Ischaemia
4
Poisoning Deliberate
4
Diabetes Mellitus
2
Intentional Overdose
2
Suicide Attempt
2
Polyuria
2
Blood Pressure Management
2
Glomerulonephritis
2
Atrial Flutter
2
Type 2 Diabetes Mellitus
2
Ischaemia
2
Migraine
2
Renal Failure
1
Hypertonia
1
Atrial Fibrillation
1
Renal Vessel Disorder
1
Dyspnoea
1
Rash
1
Electrocardiogram Abnormal
1
Hypertensive Cardiomyopathy
1
Heart Rate Irregular
1
Liver Injury
1
Coronary Artery Occlusion
1
Sleep Disorder
1
Proteinuria
1
Pain
1
Blood Cholesterol Increased
1
Completed Suicide
1
Thyroid Disorder
1
Diabetic Nephropathy
1
Muscular Weakness
1
Type 1 Diabetes Mellitus
1
Blood Cholesterol
1
Arteriosclerosis Coronary Artery
1
Blood Glucose
1
Suicidal Ideation
1

Drug Labels

LabelLabelerEffective
QuinaprilDr.Reddy's Laboratories Limited09-SEP-09
QuinaprilRanbaxy Pharmaceutical Inc.08-DEC-09
QuinaprilPhysicians Total Care, Inc.07-JAN-10
Quinapril Hydrochloride And HydrochlorothiazidePhysicians Total Care, Inc.06-MAY-10
QuinaprilSun Pharmaceutical Industries Limited01-DEC-10
Quinapril HydrochlorideMylan Pharmaceuticals Inc.21-DEC-10
QuinaprilRebel Distributors Corp04-JAN-11
Quinapril Hcl And HydrochlorothiazideGAVIS Pharmaceuticals, LLC15-JUL-11
QuinaprilCamber Pharmaceuticals26-JAN-12
Quinapril HydrochloridePD-Rx Pharmaceuticals, Inc.30-JAN-12
Quinapril AvKARE, Inc.02-AUG-12
Quinapril Hydrochloride And Hydrochlorothiazide AvKARE, Inc.02-AUG-12
Quinapril Hydrochloride/hydrochlorothiazideAurobindo Pharma Limited09-OCT-12
AccuprilParke-Davis Div of Pfizer Inc11-OCT-12
AccureticParke-Davis Div of Pfizer Inc11-OCT-12
QuinaprilBryant Ranch Prepack12-OCT-12
AccuprilBryant Ranch Prepack12-OCT-12
Quinapril Hydrochloride And HydrochlorothiazideMylan Pharmaceuticals Inc.16-OCT-12
Quinapril HydrochlorideGreenstone LLC06-NOV-12
Quinapril Hydrochloride And HydrochlorothiazideGreenstone LLC07-NOV-12
Quinapril Hydrochloride And HydrochlorothiazideCamber Pharmaceuticals14-DEC-12
QuinaprilBryant Ranch Prepack15-JAN-13
AccuprilCardinal Health09-APR-13
QuinaprilLupin Pharmaceuticals, Inc.10-APR-13
QuinaprilAurobindo Pharma Limited16-APR-13
AccuprilParke-Davis Div of Pfizer Inc02-MAY-13

Quinapril Case Reports

What Quinapril safety concerns are being reported by doctors and researchers in the medical literature?

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About Results

This report contains aggregated drug side effects and adverse events for Quinapril. The data has been pulled from the United States Food and Drug Administration's (US FDA) Adverse Event Reporting System (AERS), a database containing more than 4,000,000 adverse event reports.

DrugCite expands your query using the Unified Medical Language System (UMLS) to include generic drugs and primary active ingredients. While the core of DrugCite's advanced drug filtering algorithm is based on the industry standard UMLS, DrugCite's proprietary filtering system also includes dozens of additional steps to reconcile malformed drug names in the FDA's data.

DrugCite only counts a drug if the submitter of the adverse event indicates that the drug is suspected to have caused the adverse event.

Depending on how the data is aggregated, different counts may occur. When someone submits an adverse event to the FDA, the submitter can attribute multiple adverse events to one or more drugs. For example, an individual taking Paxil could submit the adverse events "anxiety" and "suicidal ideation" for the same individual safety report (ISR). This means when DrugCite aggregates by adverse event, two distinct adverse events are counted in the adverse event graph; once for "anxiety" and again for "suicidal ideation". However, when DrugCite aggregates by individual safety reports irrespective of the details of the adverse events contained within the safety report, the report is only counted once.

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