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CONTRAMAL

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Contramal Adverse Events Reported to the FDA Over Time

How are Contramal adverse event reports trending over time?

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

Most Common Contramal Adverse Events Reported to the FDA

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

Anaemia
20 (2.18%)
Cytolytic Hepatitis
17 (1.86%)
Malaise
17 (1.86%)
Nausea
17 (1.86%)
Confusional State
14 (1.53%)
Vomiting
14 (1.53%)
Drug Interaction
13 (1.42%)
Fall
11 (1.2%)
Febrile Bone Marrow Aplasia
10 (1.09%)
Vertigo
10 (1.09%)
Dehydration
9 (.98%)
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Hyperhidrosis
9 (.98%)
Ileitis
9 (.98%)
International Normalised Ratio Incr...
9 (.98%)
Renal Failure Acute
9 (.98%)
Thrombocytopenia
9 (.98%)
Blood Alkaline Phosphatase Increase...
8 (.87%)
Cholestasis
8 (.87%)
Condition Aggravated
8 (.87%)
Convulsion
8 (.87%)
Hallucination, Visual
8 (.87%)
Pyrexia
8 (.87%)
Alanine Aminotransferase Increased
7 (.76%)
Asthenia
7 (.76%)
Coma
7 (.76%)
Dysarthria
7 (.76%)
Facial Palsy
7 (.76%)
Haematoma
7 (.76%)
Hepatic Failure
7 (.76%)
Hepatitis Fulminant
7 (.76%)
Hypovolaemic Shock
7 (.76%)
Intestinal Obstruction
7 (.76%)
Overdose
7 (.76%)
Pruritus
7 (.76%)
Respiratory Distress
7 (.76%)
Abdominal Pain
6 (.66%)
Aspartate Aminotransferase Increase...
6 (.66%)
Gamma-glutamyltransferase Increased
6 (.66%)
Liver Function Test Abnormal
6 (.66%)
Miosis
6 (.66%)
Pancreatitis Acute
6 (.66%)
Therapeutic Agent Toxicity
6 (.66%)
Vision Blurred
6 (.66%)
Diarrhoea
5 (.55%)
Epilepsy
5 (.55%)
Hepatitis Cholestatic
5 (.55%)
Infusion Site Haemorrhage
5 (.55%)
Intestinal Ischaemia
5 (.55%)
Intra-abdominal Haematoma
5 (.55%)
Loss Of Consciousness
5 (.55%)
Sepsis
5 (.55%)
Somnolence
5 (.55%)
Accidental Overdose
4 (.44%)
Amnesia
4 (.44%)
Constipation
4 (.44%)
Cytotoxic Oedema
4 (.44%)
Drug Dependence
4 (.44%)
Encephalopathy
4 (.44%)
Eosinophilia
4 (.44%)
Face Oedema
4 (.44%)
Hemiplegia
4 (.44%)
Hypotension
4 (.44%)
Muscle Haemorrhage
4 (.44%)
Pulmonary Oedema
4 (.44%)
Rash Erythematous
4 (.44%)
Rash Maculo-papular
4 (.44%)
Syncope
4 (.44%)
Wound Haemorrhage
4 (.44%)
Abdominal Pain Upper
3 (.33%)
Acute Generalised Exanthematous Pus...
3 (.33%)
Acute Prerenal Failure
3 (.33%)
Aggression
3 (.33%)
Altered State Of Consciousness
3 (.33%)
Atrial Fibrillation
3 (.33%)
Bradycardia
3 (.33%)
Cardiac Failure
3 (.33%)
Cardiomyopathy
3 (.33%)
Cerebral Haemorrhage
3 (.33%)
Disorientation
3 (.33%)
Drug Abuser
3 (.33%)
Drug Exposure During Pregnancy
3 (.33%)
Epistaxis
3 (.33%)
Erythrosis
3 (.33%)
Gallbladder Disorder
3 (.33%)
Haematuria
3 (.33%)
Haemorrhagic Ascites
3 (.33%)
Hallucination, Auditory
3 (.33%)
Headache
3 (.33%)
Hypergammaglobulinaemia
3 (.33%)
Hypertension
3 (.33%)
Hypertonia
3 (.33%)
Hypokalaemia
3 (.33%)
Hyponatraemia
3 (.33%)
Hypothermia
3 (.33%)
Hypoxia
3 (.33%)
Lung Disorder
3 (.33%)
Mouth Haemorrhage
3 (.33%)
Mucosal Inflammation
3 (.33%)
Off Label Use
3 (.33%)
Oropharyngeal Blistering
3 (.33%)
Pain In Extremity
3 (.33%)

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

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

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

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

Drug Use For Unknown Indication
116
Pain
81
Back Pain
24
Product Used For Unknown Indication
21
Rheumatoid Arthritis
11
Sciatica
8
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Osteoarthritis
7
Headache
6
Abdominal Pain
4
Arthralgia
4
Analgesic Intervention Supportive T...
4
Chest Pain
4
Intervertebral Disc Protrusion
3
Bone Pain
3
Musculoskeletal Pain
3
Pain Prophylaxis
3
Trigeminal Neuralgia
3
Pain In Extremity
2
Drug Exposure During Pregnancy
2
Shoulder Pain
2
Psoriatic Arthropathy
2
Bile Duct Stone
2
Postoperative Analgesia
2
Procedural Pain
2
Ankylosing Spondylitis
1
Analgesic Effect
1
Teething
1
Abdominal Pain Upper
1
Ill-defined Disorder
1
Post-traumatic Headache
1
Osteoporosis
1
Pharyngitis
1
Pain Management
1
Bone Disorder
1
Cancer Pain
1
Neuralgia
1
Spinal Fracture
1
Analgesic Therapy
1
Post Herpetic Neuralgia
1
Skin Ulcer
1
Dysmenorrhoea
1
Rib Fracture
1
Pulmonary Embolism
1
Myalgia
1

Contramal Case Reports

What Contramal 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 Contramal. 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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