DrugCite
Search

NELFINAVIR MESILATE

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Nelfinavir Mesilate Adverse Events Reported to the FDA Over Time

How are Nelfinavir Mesilate adverse event reports trending over time?

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

Most Common Nelfinavir Mesilate Adverse Events Reported to the FDA

What are the most common Nelfinavir Mesilate adverse events reported to the FDA?

Drug Exposure During Pregnancy
88 (10.11%)
Abdominal Distension
23 (2.64%)
Congenital Anomaly
23 (2.64%)
Abdominal Hernia
22 (2.53%)
Cardiac Murmur
22 (2.53%)
Cryptorchism
22 (2.53%)
Lipodystrophy Acquired
18 (2.07%)
Eyelid Ptosis
17 (1.95%)
Anaemia
14 (1.61%)
Premature Baby
13 (1.49%)
Small For Dates Baby
9 (1.03%)
Show More Show More
Eyelid Function Disorder
7 (.8%)
Facial Wasting
7 (.8%)
Immune Reconstitution Syndrome
7 (.8%)
Maternal Drugs Affecting Foetus
7 (.8%)
No Adverse Event
7 (.8%)
Polydactyly
7 (.8%)
Premature Rupture Of Membranes
7 (.8%)
Atrial Septal Defect
6 (.69%)
Caesarean Section
6 (.69%)
Disseminated Intravascular Coagulat...
6 (.69%)
Foetal Distress Syndrome
6 (.69%)
Hydrocele
6 (.69%)
Intra-uterine Death
6 (.69%)
Mitochondrial Toxicity
6 (.69%)
Pulmonary Embolism
6 (.69%)
Sickle Cell Anaemia
6 (.69%)
Abortion Spontaneous
5 (.57%)
Cleft Palate
5 (.57%)
Depression
5 (.57%)
Diarrhoea
5 (.57%)
Electrocardiogram Qt Prolonged
5 (.57%)
Feeding Disorder Neonatal
5 (.57%)
Foetal Growth Retardation
5 (.57%)
Limb Malformation
5 (.57%)
Pneumocystis Jiroveci Pneumonia
5 (.57%)
Stillbirth
5 (.57%)
Trisomy 21
5 (.57%)
Brain Malformation
4 (.46%)
Diplopia
4 (.46%)
Drug Toxicity
4 (.46%)
Glucose-6-phosphate Dehydrogenase D...
4 (.46%)
Hepatic Cyst
4 (.46%)
Hepatomegaly
4 (.46%)
Hydrocephalus
4 (.46%)
Hydronephrosis
4 (.46%)
Hypospadias
4 (.46%)
Neuropathy Peripheral
4 (.46%)
Neutropenia
4 (.46%)
Pulmonary Artery Stenosis Congenita...
4 (.46%)
Retrognathia
4 (.46%)
Threatened Labour
4 (.46%)
Thrombocytopenia
4 (.46%)
Ventricular Hypertrophy
4 (.46%)
Virologic Failure
4 (.46%)
Vomiting
4 (.46%)
Arnold-chiari Malformation
3 (.34%)
Cd4 Lymphocytes Decreased
3 (.34%)
Convulsion
3 (.34%)
Dermatitis Bullous
3 (.34%)
Drug Interaction
3 (.34%)
Dysphagia
3 (.34%)
Epilepsy
3 (.34%)
Gynaecomastia
3 (.34%)
Haemangioma
3 (.34%)
Hypotonia Neonatal
3 (.34%)
Infection
3 (.34%)
Leukopenia
3 (.34%)
Mental Disorder
3 (.34%)
Microcephaly
3 (.34%)
Ophthalmoplegia
3 (.34%)
Osteonecrosis
3 (.34%)
Pancreatic Carcinoma
3 (.34%)
Paraesthesia
3 (.34%)
Peripheral Sensory Neuropathy
3 (.34%)
Portal Hypertension
3 (.34%)
Premature Labour
3 (.34%)
Progressive External Ophthalmoplegi...
3 (.34%)
Pyloric Stenosis
3 (.34%)
Respiratory Distress
3 (.34%)
Solitary Kidney
3 (.34%)
Splenomegaly
3 (.34%)
Torsade De Pointes
3 (.34%)
Trisomy 15
3 (.34%)
Ventricular Septal Defect
3 (.34%)
Adverse Drug Reaction
2 (.23%)
Apnoea
2 (.23%)
Astrocytoma
2 (.23%)
Astrocytoma, Low Grade
2 (.23%)
Atrioventricular Block Complete
2 (.23%)
Atypical Mycobacterial Infection
2 (.23%)
Body Temperature Fluctuation
2 (.23%)
Bradycardia
2 (.23%)
Bundle Branch Block Left
2 (.23%)
Candidiasis
2 (.23%)
Cholecystitis
2 (.23%)
Congenital Nystagmus
2 (.23%)
Congenital Torticollis
2 (.23%)
Cyanosis Neonatal
2 (.23%)
Death
2 (.23%)
Dermatitis Allergic
2 (.23%)

ExportShare/Embed GraphExport Export Data

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

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

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

Hiv Infection
185
Drug Exposure During Pregnancy
44
Antiretroviral Therapy
14
Hiv Test Positive
13
Drug Use For Unknown Indication
8
Acquired Immunodeficiency Syndrome
5
Show More Show More
Prophylaxis Against Hiv Infection
4
Pancreatic Carcinoma
4
Antiviral Prophylaxis
3
Prophylaxis
3
Product Used For Unknown Indication
2
Retroviral Infection
1
Hepatitis C
1

Nelfinavir Mesilate Case Reports

What Nelfinavir Mesilate 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 Nelfinavir Mesilate. 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 Nelfinavir Mesilate.