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PROCARDIA XL

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Procardia Xl Adverse Events Reported to the FDA Over Time

How are Procardia Xl adverse event reports trending over time?

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

Most Common Procardia Xl Adverse Events Reported to the FDA

What are the most common Procardia Xl adverse events reported to the FDA?

Dizziness
52 (3.45%)
Drug Ineffective
49 (3.25%)
Headache
48 (3.18%)
Hypertension
45 (2.98%)
Blood Pressure Increased
34 (2.25%)
Blood Pressure Inadequately Control...
27 (1.79%)
Asthenia
25 (1.66%)
Nausea
21 (1.39%)
Weight Decreased
20 (1.33%)
Feeling Abnormal
19 (1.26%)
Malaise
18 (1.19%)
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Oedema Peripheral
18 (1.19%)
Cerebrovascular Accident
17 (1.13%)
Death
17 (1.13%)
Diabetes Mellitus
17 (1.13%)
Anxiety
16 (1.06%)
Blood Pressure Decreased
14 (.93%)
Dyspnoea
14 (.93%)
Medication Residue
14 (.93%)
Palpitations
13 (.86%)
Asthma
12 (.8%)
Fatigue
12 (.8%)
Blood Cholesterol Increased
11 (.73%)
Cardiac Disorder
11 (.73%)
Vision Blurred
11 (.73%)
Arthritis
10 (.66%)
Blood Glucose Increased
10 (.66%)
Confusional State
10 (.66%)
Hypersensitivity
10 (.66%)
Pain In Extremity
10 (.66%)
Renal Disorder
10 (.66%)
Hearing Impaired
9 (.6%)
Hypotension
9 (.6%)
Pain
9 (.6%)
Renal Failure
9 (.6%)
Wrong Technique In Drug Usage Proce...
9 (.6%)
Blood Pressure Fluctuation
8 (.53%)
Cough
8 (.53%)
Drug Effect Decreased
8 (.53%)
Drug Intolerance
8 (.53%)
Fall
8 (.53%)
Heart Rate Increased
8 (.53%)
Hypoaesthesia
8 (.53%)
Muscle Spasms
8 (.53%)
Tremor
8 (.53%)
Weight Increased
8 (.53%)
Abdominal Pain Upper
7 (.46%)
Chest Pain
7 (.46%)
Flushing
7 (.46%)
Heart Rate Irregular
7 (.46%)
Hypoacusis
7 (.46%)
Insomnia
7 (.46%)
Joint Swelling
7 (.46%)
Nervousness
7 (.46%)
Rash
7 (.46%)
Renal Impairment
7 (.46%)
Stress
7 (.46%)
Vascular Graft
7 (.46%)
Weight Fluctuation
7 (.46%)
Depression
6 (.4%)
Disorientation
6 (.4%)
Drug Dispensing Error
6 (.4%)
Dysarthria
6 (.4%)
Facial Paresis
6 (.4%)
Gastrooesophageal Reflux Disease
6 (.4%)
Intentional Drug Misuse
6 (.4%)
Memory Impairment
6 (.4%)
Mental Status Changes
6 (.4%)
Myocardial Infarction
6 (.4%)
Pyuria
6 (.4%)
Renal Failure Acute
6 (.4%)
Somnolence
6 (.4%)
Teeth Brittle
6 (.4%)
Tooth Loss
6 (.4%)
Urinary Tract Infection
6 (.4%)
Anaphylactic Reaction
5 (.33%)
Angina Unstable
5 (.33%)
Arthralgia
5 (.33%)
Arthropod Bite
5 (.33%)
Bladder Disorder
5 (.33%)
Blood Disorder
5 (.33%)
Blood Triglycerides Increased
5 (.33%)
Breast Cancer
5 (.33%)
Drug Interaction
5 (.33%)
Dyspepsia
5 (.33%)
Dysphagia
5 (.33%)
Dysstasia
5 (.33%)
Gout
5 (.33%)
Malignant Hypertension
5 (.33%)
Medication Error
5 (.33%)
Muscular Weakness
5 (.33%)
No Adverse Event
5 (.33%)
Pruritus
5 (.33%)
Skull Fracture
5 (.33%)
Swollen Tongue
5 (.33%)
Urinary Retention
5 (.33%)
Abasia
4 (.27%)
Abdominal Discomfort
4 (.27%)
Blood Glucose Decreased
4 (.27%)
Blood Pressure Diastolic Decreased
4 (.27%)
Body Height Decreased
4 (.27%)

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This graph shows the top adverse events submitted to the FDA for Procardia Xl, 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 Procardia Xl 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 Procardia Xl

What are the most common Procardia Xl adverse events reported to the FDA?

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This graph shows the top categories of adverse events submitted to the FDA for Procardia Xl, 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 Procardia Xl 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 Procardia Xl According to Those Reporting Adverse Events

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

Hypertension
313
Drug Use For Unknown Indication
46
Product Used For Unknown Indication
36
Blood Pressure
30
Blood Pressure Abnormal
17
Cardiac Disorder
16
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Ill-defined Disorder
15
Raynauds Phenomenon
14
Angina Pectoris
9
Coronary Artery Disease
6
Malignant Hypertension
5
Chest Pain
5
Myocardial Infarction
4
Migraine
3
Cardiovascular Disorder
3
Dyspnoea
3
Blood Pressure Increased
3
Arrhythmia
2
Epistaxis
2
Atrioventricular Block
2
Hiatus Hernia
2
Essential Hypertension
2
Pulmonary Arterial Hypertension
2
Cardiac Valve Disease
2
Oesophagitis
2
Postoperative Care
2
Arterial Disorder
1
Heart Rate Irregular
1
Drug Therapy Changed
1
Peripheral Vascular Disorder
1
Peripheral Coldness
1
Hypotension
1
Gangrene
1
Blue Toe Syndrome
1
Nerve Injury
1
Blood Pressure Management
1
Thrombosis Prophylaxis
1
Skin Ulcer
1
Prophylaxis
1
Cerebrovascular Accident
1

Drug Labels

LabelLabelerEffective
Procardia XlPfizer Laboratories Div Pfizer Inc09-DEC-11
ProcardiaxlCardinal Health10-MAY-12

Procardia Xl Case Reports

What Procardia Xl 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 Procardia Xl. 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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