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ADALAT CC

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Adalat Cc Adverse Events Reported to the FDA Over Time

How are Adalat Cc adverse event reports trending over time?

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

Most Common Adalat Cc Adverse Events Reported to the FDA

What are the most common Adalat Cc adverse events reported to the FDA?

Oedema Peripheral
16 (2.02%)
Hypertension
14 (1.77%)
Pyrexia
13 (1.64%)
Hypotension
11 (1.39%)
Dyspnoea
10 (1.26%)
Back Pain
9 (1.14%)
Renal Impairment
9 (1.14%)
Asthma
8 (1.01%)
Hepatic Function Abnormal
8 (1.01%)
Medication Error
8 (1.01%)
Anaemia
7 (.88%)
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Blood Pressure Increased
7 (.88%)
Cutaneous Vasculitis
7 (.88%)
Dizziness
7 (.88%)
Drug Eruption
7 (.88%)
Interstitial Lung Disease
7 (.88%)
Psoriasis
7 (.88%)
Rash Pruritic
7 (.88%)
Altered State Of Consciousness
6 (.76%)
Blood Pressure Inadequately Control...
6 (.76%)
Cardiac Failure Chronic
6 (.76%)
Diabetes Mellitus Inadequate Contro...
6 (.76%)
Disseminated Intravascular Coagulat...
6 (.76%)
Liver Disorder
6 (.76%)
Pulmonary Congestion
6 (.76%)
Weight Increased
6 (.76%)
Angina Pectoris
5 (.63%)
Ascites
5 (.63%)
Blood Pressure Decreased
5 (.63%)
Cardiac Arrest
5 (.63%)
Cerebral Infarction
5 (.63%)
Chest Discomfort
5 (.63%)
Chest Pain
5 (.63%)
Epstein-barr Virus Infection
5 (.63%)
Flushing
5 (.63%)
Heart Rate Increased
5 (.63%)
Malaise
5 (.63%)
Multi-organ Failure
5 (.63%)
Pain
5 (.63%)
Rash
5 (.63%)
Sepsis
5 (.63%)
Tachycardia
5 (.63%)
White Blood Cell Count Decreased
5 (.63%)
Abdominal Distension
4 (.51%)
Adverse Drug Reaction
4 (.51%)
Blindness
4 (.51%)
Bradycardia
4 (.51%)
Caesarean Section
4 (.51%)
Cardio-respiratory Arrest
4 (.51%)
Cellulitis
4 (.51%)
Condition Aggravated
4 (.51%)
Erythema
4 (.51%)
Eye Haemorrhage
4 (.51%)
Feeling Hot
4 (.51%)
Haematemesis
4 (.51%)
Insomnia
4 (.51%)
Lymphoma
4 (.51%)
Neutropenia
4 (.51%)
Nocturia
4 (.51%)
Oedema
4 (.51%)
Orthostatic Hypotension
4 (.51%)
Platelet Count Decreased
4 (.51%)
Pleural Effusion
4 (.51%)
Pollakiuria
4 (.51%)
Prostatitis
4 (.51%)
Tinnitus
4 (.51%)
Toxic Skin Eruption
4 (.51%)
Vision Blurred
4 (.51%)
Abnormal Behaviour
3 (.38%)
Adverse Event
3 (.38%)
Agranulocytosis
3 (.38%)
Arthralgia
3 (.38%)
Asthenia
3 (.38%)
Blood Creatinine Increased
3 (.38%)
Blood Pressure Abnormal
3 (.38%)
Blood Urea Increased
3 (.38%)
Cardiac Failure
3 (.38%)
Cardiogenic Shock
3 (.38%)
Cleft Lip
3 (.38%)
Cleft Palate
3 (.38%)
Clonic Convulsion
3 (.38%)
Drug Ineffective
3 (.38%)
Dyskinesia
3 (.38%)
Electrocardiogram St Segment Depres...
3 (.38%)
Fall
3 (.38%)
Fluid Retention
3 (.38%)
Foetal Disorder
3 (.38%)
Gingival Swelling
3 (.38%)
Medication Residue
3 (.38%)
Mental Impairment
3 (.38%)
Muscle Spasms
3 (.38%)
No Adverse Event
3 (.38%)
Palpitations
3 (.38%)
Protein Urine Present
3 (.38%)
Pruritus
3 (.38%)
Sensory Integrative Dysfunction
3 (.38%)
Shock
3 (.38%)
Skin Exfoliation
3 (.38%)
Transient Ischaemic Attack
3 (.38%)
Tremor
3 (.38%)
Umbilical Cord Vascular Disorder
3 (.38%)

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This graph shows the top adverse events submitted to the FDA for Adalat Cc, 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 Adalat Cc 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 Adalat Cc

What are the most common Adalat Cc adverse events reported to the FDA?

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

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

Hypertension
849
Drug Use For Unknown Indication
81
Product Used For Unknown Indication
55
Essential Hypertension
17
Blood Pressure
6
Blood Pressure Increased
6
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Angina Pectoris
5
Metastases To Thorax
4
Myocardial Infarction
4
Angina Unstable
4
Oncologic Complication
3
Renal Hypertension
3
Raynauds Phenomenon
3
Unevaluable Event
3
Cardiac Failure Congestive
3
Blood Pressure Management
3
Procedural Hypertension
2
Prophylaxis
2
Blood Pressure Abnormal
2
Pulmonary Hypertension
2
Cardiac Failure
2
Cerebral Infarction
1
Arteriosclerosis Coronary Artery
1
Pain
1
Cardiac Failure Chronic
1
Anal Fissure
1
Premature Labour
1

Drug Labels

LabelLabelerEffective
Adalat CcSchering Corporation28-FEB-11
Adalat CcBayer HealthCare Pharmaceuticals Inc.08-APR-11

Adalat Cc Case Reports

What Adalat Cc 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 Adalat Cc. 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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