DrugCite
Search

ISCOTIN

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Iscotin Adverse Events Reported to the FDA Over Time

How are Iscotin adverse event reports trending over time?

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

Most Common Iscotin Adverse Events Reported to the FDA

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

Hepatic Function Abnormal
23 (2.8%)
Aspartate Aminotransferase Increase...
19 (2.31%)
Condition Aggravated
17 (2.07%)
Liver Disorder
17 (2.07%)
Alanine Aminotransferase Increased
16 (1.95%)
Disseminated Intravascular Coagulat...
16 (1.95%)
Hepatitis B
16 (1.95%)
Hepatorenal Syndrome
12 (1.46%)
Malaise
12 (1.46%)
Pneumocystis Jiroveci Pneumonia
11 (1.34%)
Pyrexia
10 (1.22%)
Show More Show More
Sepsis
10 (1.22%)
White Blood Cell Count Decreased
10 (1.22%)
Hepatitis Acute
9 (1.09%)
Rash
9 (1.09%)
Infection
8 (.97%)
Pancytopenia
8 (.97%)
Pneumonia
8 (.97%)
Renal Disorder
8 (.97%)
Renal Failure
8 (.97%)
Headache
7 (.85%)
Hepatic Encephalopathy
7 (.85%)
Hepatic Failure
7 (.85%)
Neuropathy Peripheral
7 (.85%)
Platelet Count Decreased
7 (.85%)
Abortion Missed
6 (.73%)
Anorexia
6 (.73%)
Blood Lactate Dehydrogenase Increas...
6 (.73%)
Dyspnoea
6 (.73%)
Erythema Multiforme
6 (.73%)
Hepatitis Fulminant
6 (.73%)
Quadriplegia
6 (.73%)
Vomiting
6 (.73%)
Agranulocytosis
5 (.61%)
Calculus Urinary
5 (.61%)
Drug Ineffective
5 (.61%)
Epstein-barr Virus Infection
5 (.61%)
Herpes Zoster Disseminated
5 (.61%)
Jaundice
5 (.61%)
Multi-organ Failure
5 (.61%)
Pulmonary Tuberculosis
5 (.61%)
Renal Impairment
5 (.61%)
Spinal Fracture
5 (.61%)
Systemic Lupus Erythematosus
5 (.61%)
Acute Hepatic Failure
4 (.49%)
Anaemia
4 (.49%)
Blood Alkaline Phosphatase Increase...
4 (.49%)
Blood Creatine Phosphokinase Increa...
4 (.49%)
Death
4 (.49%)
Drug Interaction
4 (.49%)
Gamma-glutamyltransferase Increased
4 (.49%)
Hepatitis
4 (.49%)
Hypersensitivity
4 (.49%)
Hypoglycaemia
4 (.49%)
Hyponatraemia
4 (.49%)
Lymphoma
4 (.49%)
Mycobacterium Avium Complex Infecti...
4 (.49%)
Pleural Effusion
4 (.49%)
Renal Failure Acute
4 (.49%)
Respiratory Failure
4 (.49%)
Adverse Drug Reaction
3 (.36%)
Aplasia Pure Red Cell
3 (.36%)
Arthritis
3 (.36%)
Ascites
3 (.36%)
Blood Bilirubin Increased
3 (.36%)
Blood Pressure Increased
3 (.36%)
Blood Urea Increased
3 (.36%)
C-reactive Protein Increased
3 (.36%)
Chest X-ray Abnormal
3 (.36%)
Chills
3 (.36%)
Cytomegalovirus Viraemia
3 (.36%)
Decreased Appetite
3 (.36%)
Diarrhoea
3 (.36%)
Drug Eruption
3 (.36%)
Drug Exposure During Pregnancy
3 (.36%)
Encephalopathy
3 (.36%)
Enteritis Infectious
3 (.36%)
Foreign Body Trauma
3 (.36%)
Glucose Urine Present
3 (.36%)
Haemodialysis
3 (.36%)
Haemolytic Anaemia
3 (.36%)
Henoch-schonlein Purpura
3 (.36%)
Immunosuppressant Drug Level Decrea...
3 (.36%)
Interstitial Lung Disease
3 (.36%)
Leukopenia
3 (.36%)
Lupus Nephritis
3 (.36%)
Nausea
3 (.36%)
Nephrotic Syndrome
3 (.36%)
Neutrophil Count Decreased
3 (.36%)
Oedema Peripheral
3 (.36%)
Optic Neuritis
3 (.36%)
Ovarian Cancer
3 (.36%)
Peritoneal Tuberculosis
3 (.36%)
Protein-losing Gastroenteropathy
3 (.36%)
Red Blood Cell Count Decreased
3 (.36%)
Rheumatoid Arthritis
3 (.36%)
Rhinorrhoea
3 (.36%)
Scotoma
3 (.36%)
Urinary Tract Infection
3 (.36%)
Uterine Cancer
3 (.36%)
Weight Increased
3 (.36%)

ExportShare/Embed GraphExport Export Data

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

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

Show More Show More

ExportShare/Embed Graph Export Export Data

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

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

Antibiotic Prophylaxis
448
Prophylaxis
78
Pulmonary Tuberculosis
43
Tuberculosis
35
Drug Use For Unknown Indication
26
Tuberculosis Prophylaxis
22
Show More Show More
Lymph Node Tuberculosis
20
Disseminated Tuberculosis
13
Tuberculous Pleurisy
12
Infection Prophylaxis
6
Latent Tuberculosis
6
Rheumatoid Arthritis
5
Pneumonia
5
Atypical Mycobacterial Infection
4
Product Used For Unknown Indication
4
Mycobacterium Avium Complex Infecti...
4
Pleural Effusion
3
Meningitis Tuberculous
3
Cutaneous Tuberculosis
2
Infection
2
Renal Transplant
2
Bronchitis Chronic
2
Pneumocystis Jiroveci Pneumonia
2
Tuberculin Test Positive
2
Chest X-ray Abnormal
1
Fungal Infection
1
Bacterial Disease Carrier
1
Pericarditis Tuberculous
1
Juvenile Arthritis
1
Hiv Infection
1
Pneumonia Bacterial
1
Ear Tuberculosis
1
Spinal Disorder
1
Tuberculosis Test Positive
1
Lymphadenitis
1
Drug Exposure During Pregnancy
1
Ill-defined Disorder
1

Iscotin Case Reports

What Iscotin safety concerns are being reported by doctors and researchers in the medical literature?

Powered by Google

About Results

This report contains aggregated drug side effects and adverse events for Iscotin. 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.

Comments

Share your experience with Iscotin.