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LISINOPRIL AND HYDROCHLOROTHIAZIDE

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Lisinopril And Hydrochlorothiazide Adverse Events Reported to the FDA Over Time

How are Lisinopril And Hydrochlorothiazide adverse event reports trending over time?

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

Most Common Lisinopril And Hydrochlorothiazide Adverse Events Reported to the FDA

What are the most common Lisinopril And Hydrochlorothiazide adverse events reported to the FDA?

Angioedema
212 (5.1%)
Cough
128 (3.08%)
Dizziness
92 (2.21%)
Renal Failure Acute
75 (1.81%)
Fatigue
62 (1.49%)
Dyspnoea
59 (1.42%)
Nausea
56 (1.35%)
Hypotension
54 (1.3%)
Drug Ineffective
50 (1.2%)
Blood Pressure Increased
46 (1.11%)
Completed Suicide
43 (1.04%)
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Dehydration
42 (1.01%)
Hypoaesthesia
40 (.96%)
Diarrhoea
38 (.91%)
Swollen Tongue
38 (.91%)
Headache
37 (.89%)
Pain
37 (.89%)
Syncope
37 (.89%)
Asthenia
36 (.87%)
Dysphagia
36 (.87%)
Hypertension
36 (.87%)
Pruritus
34 (.82%)
Malaise
32 (.77%)
Swelling Face
32 (.77%)
Paraesthesia
31 (.75%)
Muscle Spasms
30 (.72%)
Insomnia
28 (.67%)
Vomiting
28 (.67%)
Feeling Abnormal
26 (.63%)
Rash
26 (.63%)
Arthralgia
25 (.6%)
Blood Creatinine Increased
25 (.6%)
Confusional State
25 (.6%)
Back Pain
24 (.58%)
Lip Swelling
24 (.58%)
Burning Sensation
23 (.55%)
Hypersensitivity
23 (.55%)
Hyponatraemia
23 (.55%)
Drug Interaction
22 (.53%)
Product Substitution Issue
22 (.53%)
Chest Pain
21 (.51%)
Pharyngeal Oedema
21 (.51%)
Drug Hypersensitivity
20 (.48%)
Cardiac Arrest
19 (.46%)
Gait Disturbance
19 (.46%)
Hyperhidrosis
19 (.46%)
Vision Blurred
19 (.46%)
Heart Rate Increased
18 (.43%)
Hyperkalaemia
18 (.43%)
Medication Error
18 (.43%)
Muscular Weakness
18 (.43%)
Musculoskeletal Pain
18 (.43%)
Respiratory Arrest
17 (.41%)
Urosepsis
17 (.41%)
Urticaria
17 (.41%)
Weight Increased
17 (.41%)
Blood Pressure Decreased
16 (.39%)
Fall
16 (.39%)
Pain In Extremity
16 (.39%)
Tremor
16 (.39%)
Abdominal Pain Upper
15 (.36%)
Blood Glucose Increased
15 (.36%)
Somnolence
15 (.36%)
Breast Swelling
14 (.34%)
Loss Of Consciousness
14 (.34%)
Product Quality Issue
14 (.34%)
Speech Disorder
14 (.34%)
Blood Pressure Systolic Increased
13 (.31%)
Death
13 (.31%)
Fluid Overload
13 (.31%)
Palpitations
13 (.31%)
Renal Failure
13 (.31%)
Abdominal Pain
12 (.29%)
Decreased Appetite
12 (.29%)
Dyskinesia
12 (.29%)
Hypokalaemia
12 (.29%)
Myalgia
12 (.29%)
Oedema Peripheral
12 (.29%)
Throat Irritation
12 (.29%)
Weight Decreased
12 (.29%)
Blood Sodium Decreased
11 (.26%)
Chest Discomfort
11 (.26%)
Coagulation Factor Viii Level Decre...
11 (.26%)
Coagulation Time Prolonged
11 (.26%)
Dysphonia
11 (.26%)
Haematoma
11 (.26%)
Intentional Drug Misuse
11 (.26%)
Neck Pain
11 (.26%)
Pneumonia
11 (.26%)
Rash Erythematous
11 (.26%)
Unresponsive To Stimuli
11 (.26%)
Wheezing
11 (.26%)
Abdominal Discomfort
10 (.24%)
Condition Aggravated
10 (.24%)
Depressed Level Of Consciousness
10 (.24%)
Depression
10 (.24%)
Dialysis
10 (.24%)
Intentional Overdose
10 (.24%)
Lactic Acidosis
10 (.24%)
Oropharyngeal Pain
10 (.24%)
Pancreatitis
10 (.24%)

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This graph shows the top adverse events submitted to the FDA for Lisinopril And Hydrochlorothiazide, 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 Lisinopril And Hydrochlorothiazide 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 Lisinopril And Hydrochlorothiazide

What are the most common Lisinopril And Hydrochlorothiazide adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Lisinopril And Hydrochlorothiazide, 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 Lisinopril And Hydrochlorothiazide 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 Lisinopril And Hydrochlorothiazide According to Those Reporting Adverse Events

Why are people taking Lisinopril And Hydrochlorothiazide, according to those reporting adverse events to the FDA?

Hypertension
1359
Product Used For Unknown Indication
267
Blood Pressure
118
Drug Use For Unknown Indication
98
Blood Pressure Increased
47
Blood Pressure Abnormal
46
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Cardiac Disorder
14
Fluid Retention
10
Essential Hypertension
8
Blood Pressure Management
7
Diuretic Therapy
6
Diabetes Mellitus
6
Atrial Fibrillation
5
Oedema
4
Coronary Artery Disease
4
Cardiac Failure Congestive
4
Oedema Peripheral
3
Hypotension
3
Blood Cholesterol
3
Ill-defined Disorder
2
Glucose Tolerance Impaired
2
Hypertensive Heart Disease
2
Drug Hypersensitivity
2
Angioedema
2
Polycythaemia
1
Dyspnoea
1
Cardiac Valve Disease
1
Chest Pain
1
Polyuria
1
Intentional Overdose
1
Prostate Cancer
1
Completed Suicide
1
Coronary Artery Bypass
1
Swelling
1
Diabetic Complication
1
Pain
1
Aortic Disorder
1
Anticoagulant Therapy
1
Blood Pressure Decreased
1
Cough
1
Prehypertension
1
Malignant Hypertension
1
Left Ventricular Hypertrophy
1
Drug Ineffective
1
Cardiac Failure
1
Myocardial Infarction
1
Renal Failure Chronic
1
Angina Pectoris
1
Proteinuria
1

Drug Labels

LabelLabelerEffective
Lisinopril And HydrochlorothiazidePhysicians Total Care, Inc.22-SEP-09
Lisinopril And HydrochlorothiazideUDL Laboratories, Inc.15-DEC-09
Lisinopril With HydrochlorothiazideH.J. Harkins Company, Inc.01-JAN-10
Lisinopril And HydrochlorothiazideState of Florida DOH Central Pharmacy07-JUN-10
Lisinopril And HydrochlorothiazideState of Florida DOH Central Pharmacy07-JUN-10
Lisinopril And HydrochlorothiazidePD-Rx Pharmaceuticals, Inc.04-AUG-10
Lisinopril And HydrochlorothiazideLake Erie medical DBA Quality Care Products LLC11-AUG-10
Lisinopril And HydrochlorothiazideRebel Distributors Corp01-OCT-10
Lisinopril And HydrochlorothiazideBlenheim Pharmacal, Inc.06-OCT-10
Lisinopril And HydrochlorothiazideREMEDYREPACK INC. 28-MAR-11
Lisinopril And HydrochlorothiazideREMEDYREPACK INC. 28-MAR-11
Lisinopril And Hydrochlorothiazide Preferred Pharmaceuticals, Inc31-MAR-11
Lisinopril And HydrochlorothiazideREMEDYREPACK INC. 22-APR-11
Lisinopril And HydrochlorothiazideREMEDYREPACK INC. 04-MAY-11
Lisinopril And HydrochlorothiazideREMEDYREPACK INC. 06-JUN-11
Lisinopril And HydrochlorothiazideREMEDYREPACK INC. 12-SEP-11
Lisinopril And HydrochlorothiazideAurobindo Pharma Limited14-SEP-11
Lisinopril With HydrochlorothiazidePD-Rx Pharmaceuticals, Inc.15-SEP-11
Lisinopril With HydrochlorothiazidePD-Rx Pharmaceuticals, Inc.15-SEP-11
Lisinopril With HydrochlorothiazidePD-Rx Pharmaceuticals, Inc.15-SEP-11
Lisinopril And HydrochlorothiazideEon Labs, Inc.21-SEP-11
Lisinopril And HydrochlorothiazideREMEDYREPACK INC. 31-OCT-11
Lisinopril And HydrochlorothiazideDispensing Solutions, Inc.07-NOV-11
Lisinopril With HydrochlorothiazideGolden State Medical Supply, Inc.09-JAN-12
Lisinopril And HydrochlorothiazideInternational Labs, Inc.03-APR-12
Lisinopril And HydrochlorothiazidePreferred Pharmaceuticals, Inc23-APR-12
Lisinopril With HydrochlorothiazideWest-ward Pharmaceutical Corp23-MAY-12
Lisinopril And HydrochlorothiazideAmerican Health Packaging29-JUN-12
Lisinopril And HydrochlorothiazideLake Erie Medical & Surgical Supply DBA Quality Care Products LLC31-JUL-12
Lisinopril And HydrochlorothiazideLupin Pharmaceuticals, Inc.09-AUG-12
Lisinopril And HydrochlorothiazideInternational Labs, Inc.19-SEP-12
Lisinopril And Hydrochlorothiazide STAT Rx USA LLC24-SEP-12
Lisinopril And HydrochlorothiazideGreenstone LLC06-OCT-12
Lisinopril And HydrochlorothiazideBryant Ranch Prepack12-OCT-12
Lisinopril And HydrochlorothiazideBryant Ranch Prepack12-OCT-12
ZestoreticAstraZeneca Pharmaceuticals LP31-OCT-12
Lisinopril And HydrochlorothiazideLake Erie Medical DBA Quality Care Products LLC09-NOV-12
Lisinopril And HydrochlorothiazideInternational Labs, Inc.03-DEC-12
Lisinopril And HydrochlorothiazideIVAX Pharmaceuticals, Inc.07-DEC-12
Lisinopril And HydrochlorothiazideMylan Pharmaceuticals Inc.13-DEC-12
Lisinopril And HydrochlorothiazideBryant Ranch Prepack18-JAN-13
Lisinopril And HydrochlorothiazideApotex Corp.30-JAN-13
Lisinopril And HydrochlorothiazideWatson Laboratories, Inc.04-FEB-13
Lisinopril And HydrochlorothiazideNCS HealthCare of KY, Inc dba Vangard Labs25-FEB-13
Lisinopril-hydrochlorothiazideRanbaxy Pharmaceuticals Inc.07-MAR-13

Lisinopril And Hydrochlorothiazide Case Reports

What Lisinopril And Hydrochlorothiazide 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 Lisinopril And Hydrochlorothiazide. 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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