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Clinoril Adverse Events Reported to the FDA Over Time

How are Clinoril adverse event reports trending over time?

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

Most Common Clinoril Adverse Events Reported to the FDA

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

Diarrhoea
18 (2.11%)
Renal Impairment
18 (2.11%)
Drug Exposure During Pregnancy
14 (1.64%)
Sepsis
12 (1.41%)
Gastrointestinal Haemorrhage
11 (1.29%)
Renal Failure Acute
11 (1.29%)
Constipation
10 (1.17%)
Hyperkalaemia
10 (1.17%)
Pyrexia
10 (1.17%)
Anorexia
9 (1.06%)
Gastrointestinal Mucosal Disorder
9 (1.06%)
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Renal Disorder
9 (1.06%)
Acidosis
8 (.94%)
Anaphylactic Shock
8 (.94%)
Cholangitis
8 (.94%)
Condition Aggravated
8 (.94%)
Enteritis
8 (.94%)
Ileal Ulcer Perforation
8 (.94%)
Malaise
8 (.94%)
Pneumocystis Jiroveci Pneumonia
8 (.94%)
Disseminated Intravascular Coagulat...
7 (.82%)
Haemodialysis
7 (.82%)
Pancreatitis Acute
7 (.82%)
Premature Baby
7 (.82%)
Toxic Epidermal Necrolysis
7 (.82%)
Urticaria
7 (.82%)
Abdominal Pain
6 (.7%)
Anaemia
6 (.7%)
Autoimmune Hepatitis
6 (.7%)
Dehydration
6 (.7%)
Gastric Ulcer
6 (.7%)
Hepatic Cirrhosis
6 (.7%)
Hepatic Failure
6 (.7%)
Hydronephrosis
6 (.7%)
Hypotension
6 (.7%)
Liver Disorder
6 (.7%)
Metabolic Acidosis
6 (.7%)
Peritonitis
6 (.7%)
Portal Venous Gas
6 (.7%)
Respiratory Failure
6 (.7%)
White Blood Cell Count Increased
6 (.7%)
Ascites
5 (.59%)
Back Pain
5 (.59%)
Blood Lactate Dehydrogenase Increas...
5 (.59%)
Caesarean Section
5 (.59%)
Dyspnoea
5 (.59%)
Gastric Mucosal Lesion
5 (.59%)
Jaundice
5 (.59%)
Pancreatitis
5 (.59%)
Platelet Count Decreased
5 (.59%)
Rash
5 (.59%)
Renal Failure
5 (.59%)
Adverse Event
4 (.47%)
Altered State Of Consciousness
4 (.47%)
Arteriosclerosis
4 (.47%)
Arthralgia
4 (.47%)
Cholestasis
4 (.47%)
Drug Hypersensitivity
4 (.47%)
Drug Rash With Eosinophilia And Sys...
4 (.47%)
Fluid Retention
4 (.47%)
Gastric Cancer
4 (.47%)
Gastritis
4 (.47%)
Haemoglobin Decreased
4 (.47%)
Herpes Zoster
4 (.47%)
Hypertrophy
4 (.47%)
Intestinal Ischaemia
4 (.47%)
Lactose Intolerance
4 (.47%)
Neuropathy Peripheral
4 (.47%)
Palmar-plantar Erythrodysaesthesia ...
4 (.47%)
Pancreatitis Chronic
4 (.47%)
Proctalgia
4 (.47%)
Rectal Perforation
4 (.47%)
Shock Haemorrhagic
4 (.47%)
Abdominal Distension
3 (.35%)
Abdominal Pain Upper
3 (.35%)
C-reactive Protein Increased
3 (.35%)
Cardiac Failure
3 (.35%)
Cardiac Failure Congestive
3 (.35%)
Chronic Obstructive Pulmonary Disea...
3 (.35%)
Colitis Ischaemic
3 (.35%)
Desmoid Tumour
3 (.35%)
Dizziness
3 (.35%)
Drug Eruption
3 (.35%)
Drug Toxicity
3 (.35%)
Gastric Ulcer Haemorrhage
3 (.35%)
General Physical Health Deteriorati...
3 (.35%)
Headache
3 (.35%)
Hepatitis Toxic
3 (.35%)
Infection
3 (.35%)
Intentional Drug Misuse
3 (.35%)
Interstitial Lung Disease
3 (.35%)
Liver Abscess
3 (.35%)
Muscle Spasms
3 (.35%)
Nausea
3 (.35%)
Ocular Hyperaemia
3 (.35%)
Osteomyelitis
3 (.35%)
Pain
3 (.35%)
Pancytopenia
3 (.35%)
Pleural Effusion
3 (.35%)
Pseudomonal Bacteraemia
3 (.35%)
Pyloric Stenosis
3 (.35%)

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

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

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

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

Rheumatoid Arthritis
139
Arthritis
26
Pain
22
Drug Use For Unknown Indication
15
Back Pain
14
Arthralgia
14
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Product Used For Unknown Indication
12
Osteoarthritis
7
Polyhydramnios
7
Antiinflammatory Therapy
6
Sle Arthritis
6
Monarthritis
5
Inflammation
4
Nephrolithiasis
4
Scleroderma
4
Osteoporosis
4
Prophylaxis
4
Neck Mass
3
Adenomatous Polyposis Coli
3
Feeling Abnormal
3
Chondrocalcinosis Pyrophosphate
3
Pyrexia
3
Musculoskeletal Pain
3
Cervicobrachial Syndrome
2
Pain In Extremity
2
Dysmenorrhoea
2
Osteonecrosis
2
Cancer Pain
2
Prostatitis
2
Juvenile Arthritis
2
Chemotherapy
1
Herpes Simplex
1
Analgesic Therapy
1
Intervertebral Disc Protrusion
1
Nasopharyngitis
1
Gout
1
Myalgia
1
Tendonitis
1
Desmoid Tumour
1
Psoriatic Arthropathy
1
Behcets Syndrome
1
Systemic Lupus Erythematosus
1
Neck Pain
1
Hypertension
1
Iritis
1
Psoriasis
1
Flank Pain
1
Neoplasm Malignant
1

Clinoril Case Reports

What Clinoril 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 Clinoril. 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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