DrugCite
Search

ABELCET

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Abelcet Adverse Events Reported to the FDA Over Time

How are Abelcet adverse event reports trending over time?

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

Most Common Abelcet Adverse Events Reported to the FDA

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

Chills
52 (5.66%)
Tachycardia
47 (5.11%)
Hypertension
33 (3.59%)
Pyrexia
33 (3.59%)
Oxygen Saturation Decreased
22 (2.39%)
Blood Pressure Increased
21 (2.29%)
Infusion Related Reaction
20 (2.18%)
Tachypnoea
19 (2.07%)
Heart Rate Increased
18 (1.96%)
Tremor
17 (1.85%)
Renal Failure
14 (1.52%)
Show More Show More
Blood Creatinine Increased
13 (1.41%)
Hypokalaemia
11 (1.2%)
Body Temperature Increased
9 (.98%)
Condition Aggravated
9 (.98%)
Hypotension
9 (.98%)
Renal Failure Acute
9 (.98%)
Respiratory Failure
9 (.98%)
Respiratory Rate Increased
9 (.98%)
Cyanosis
8 (.87%)
Dyspnoea
8 (.87%)
Pancytopenia
8 (.87%)
Convulsion
7 (.76%)
Nephrogenic Diabetes Insipidus
7 (.76%)
Rash
7 (.76%)
Renal Impairment
7 (.76%)
Blood Glucose Increased
6 (.65%)
Blood Pressure Decreased
6 (.65%)
Febrile Neutropenia
6 (.65%)
Respiratory Distress
6 (.65%)
Thrombocytopenia
6 (.65%)
Acidosis
5 (.54%)
Blood Bicarbonate Decreased
5 (.54%)
Cardio-respiratory Arrest
5 (.54%)
Drug Ineffective
5 (.54%)
Hyperventilation
5 (.54%)
Lymphadenopathy
5 (.54%)
Multi-organ Failure
5 (.54%)
Peripheral Coldness
5 (.54%)
Acute Myocardial Infarction
4 (.44%)
Agitation
4 (.44%)
Alanine Aminotransferase Increased
4 (.44%)
Aspergillosis
4 (.44%)
Atrial Fibrillation
4 (.44%)
Blood Potassium Decreased
4 (.44%)
Blood Sodium Decreased
4 (.44%)
Blood Urea Increased
4 (.44%)
Bronchospasm
4 (.44%)
Disease Progression
4 (.44%)
Hepatosplenomegaly
4 (.44%)
Hyperamylasaemia
4 (.44%)
Nephropathy Toxic
4 (.44%)
Ventricular Extrasystoles
4 (.44%)
Wheezing
4 (.44%)
Acute Pulmonary Oedema
3 (.33%)
Anaemia
3 (.33%)
Ascites
3 (.33%)
Aspartate Aminotransferase Increase...
3 (.33%)
Blood Bilirubin Increased
3 (.33%)
Cardiac Death
3 (.33%)
Feeling Cold
3 (.33%)
General Physical Health Deteriorati...
3 (.33%)
Headache
3 (.33%)
Hyperbilirubinaemia
3 (.33%)
Hyperkalaemia
3 (.33%)
Hypothermia
3 (.33%)
Hypoxia
3 (.33%)
Ileus Paralytic
3 (.33%)
Liver Function Test Abnormal
3 (.33%)
Nausea
3 (.33%)
Neutropenia
3 (.33%)
No Therapeutic Response
3 (.33%)
Pneumonia
3 (.33%)
Pulmonary Embolism
3 (.33%)
Pulmonary Oedema
3 (.33%)
Sepsis
3 (.33%)
Staphylococcal Bacteraemia
3 (.33%)
Vomiting
3 (.33%)
Aplastic Anaemia
2 (.22%)
Autonomic Nervous System Imbalance
2 (.22%)
Blindness
2 (.22%)
Blood Alkaline Phosphatase Increase...
2 (.22%)
Blood Chloride Increased
2 (.22%)
Blood Culture Positive
2 (.22%)
Blood Sodium Increased
2 (.22%)
Bradycardia
2 (.22%)
Bronchopulmonary Aspergillosis
2 (.22%)
Cardiac Arrest
2 (.22%)
Catheter Related Complication
2 (.22%)
Central Line Infection
2 (.22%)
Cerebral Infarction
2 (.22%)
Cerebral Toxoplasmosis
2 (.22%)
Cholestasis
2 (.22%)
Coma
2 (.22%)
Deafness
2 (.22%)
Death
2 (.22%)
Diabetes Insipidus
2 (.22%)
Dialysis
2 (.22%)
Diarrhoea
2 (.22%)
Drug Interaction
2 (.22%)
Drug Level Below Therapeutic
2 (.22%)

ExportShare/Embed GraphExport Export Data

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

What are the most common Abelcet 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 Abelcet, 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 Abelcet 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 Abelcet According to Those Reporting Adverse Events

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

Product Used For Unknown Indication
35
Fungal Infection
29
Aspergillosis
23
Antifungal Prophylaxis
16
Drug Use For Unknown Indication
16
Bronchopulmonary Aspergillosis
13
Show More Show More
Candidiasis
11
Meningitis Cryptococcal
9
Febrile Neutropenia
8
Prophylaxis
8
Sepsis
8
Zygomycosis
7
Mucormycosis
7
Evidence Based Treatment
6
Meningitis
5
Pneumonia Fungal
4
Cryptococcosis
4
Pyrexia
3
Pneumonia
3
Lung Infection
3
Oesophageal Candidiasis
3
Systemic Candida
2
Coccidioidomycosis
2
Candida Sepsis
2
Histoplasmosis
2
Bone Marrow Failure
2
Neutrophilia
2
Acute Myeloid Leukaemia
2
Acute Lymphocytic Leukaemia
2
Nervous System Disorder
2
Infection
2
Febrile Bone Marrow Aplasia
2
Respiratory Tract Infection Fungal
2
Systemic Mycosis
2
Pulmonary Mycosis
2
Abdominal Sepsis
1
Lung Transplant
1
Upper Respiratory Fungal Infection
1
Culture Urine Positive
1
Urinary Tract Infection
1
Fusarium Infection
1
Lung Disorder
1
Respiratory Moniliasis
1
Antifungal Treatment
1
Meningitis Fungal
1
Fungal Peritonitis
1
Ill-defined Disorder
1
Respiratory Disorder
1
Leishmaniasis
1
Fungus Urine Test Positive
1
Acute Respiratory Distress Syndrome
1

Drug Labels

LabelLabelerEffective
AbelcetSigma-Tau Pharmaceuticals, Inc.08-JUN-12

Abelcet Case Reports

What Abelcet 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 Abelcet. 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 Abelcet.