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INDINIVIR SULFATE

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Indinivir Sulfate Adverse Events Reported to the FDA Over Time

How are Indinivir Sulfate adverse event reports trending over time?

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

Most Common Indinivir Sulfate Adverse Events Reported to the FDA

What are the most common Indinivir Sulfate adverse events reported to the FDA?

Lipodystrophy Acquired
35 (4.05%)
Portal Hypertension
23 (2.66%)
Eyelid Ptosis
19 (2.2%)
Abdominal Distension
14 (1.62%)
Diplopia
14 (1.62%)
Immune Reconstitution Syndrome
14 (1.62%)
Mitochondrial Toxicity
14 (1.62%)
Progressive External Ophthalmoplegi...
14 (1.62%)
Portal Vein Thrombosis
13 (1.5%)
Hepatic Failure
11 (1.27%)
Blood Lactic Acid Increased
10 (1.16%)
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Lactic Acidosis
10 (1.16%)
Portal Hypertensive Gastropathy
10 (1.16%)
Sepsis
10 (1.16%)
Abdominal Pain
9 (1.04%)
Constipation
9 (1.04%)
Mitochondrial Cytopathy
9 (1.04%)
Candidiasis
8 (.93%)
Drug Resistance
8 (.93%)
Malignant Melanoma
8 (.93%)
Pulmonary Hypertension
8 (.93%)
Varices Oesophageal
8 (.93%)
Blood Creatine Phosphokinase Increa...
7 (.81%)
Drug Exposure During Pregnancy
7 (.81%)
Escherichia Infection
7 (.81%)
Hypoventilation
7 (.81%)
Metastases To Lymph Nodes
7 (.81%)
Nodular Regenerative Hyperplasia
7 (.81%)
Pyrexia
7 (.81%)
Abdominal Hernia
6 (.69%)
Cardiac Murmur
6 (.69%)
Cryptorchism
6 (.69%)
Metastases To Skin
6 (.69%)
Virologic Failure
6 (.69%)
Anaemia
5 (.58%)
Aspartate Aminotransferase Increase...
5 (.58%)
Blood Creatinine Increased
5 (.58%)
Congenital Anomaly
5 (.58%)
Diarrhoea
5 (.58%)
Nephrolithiasis
5 (.58%)
Neuropathy Peripheral
5 (.58%)
Oesophageal Varices Haemorrhage
5 (.58%)
Ophthalmoplegia
5 (.58%)
Pneumocystis Jiroveci Pneumonia
5 (.58%)
Pneumonia
5 (.58%)
Progressive Multifocal Leukoencepha...
5 (.58%)
Rash
5 (.58%)
Splenomegaly
5 (.58%)
Ascites
4 (.46%)
Blood Hiv Rna Increased
4 (.46%)
Blood Ph Abnormal
4 (.46%)
Bundle Branch Block Left
4 (.46%)
Cd4 Lymphocytes Decreased
4 (.46%)
Drug Toxicity
4 (.46%)
Fatigue
4 (.46%)
Hyperlipidaemia
4 (.46%)
Lipoatrophy
4 (.46%)
Myalgia
4 (.46%)
Neoplasm Malignant
4 (.46%)
Oesophageal Candidiasis
4 (.46%)
Osteonecrosis
4 (.46%)
Renal Failure
4 (.46%)
Supraventricular Tachycardia
4 (.46%)
Viral Mutation Identified
4 (.46%)
Acute Chest Syndrome
3 (.35%)
Acute Respiratory Distress Syndrome
3 (.35%)
Asthenia
3 (.35%)
Blood Ph Decreased
3 (.35%)
Cachexia
3 (.35%)
Confusional State
3 (.35%)
Depression
3 (.35%)
Drug Ineffective
3 (.35%)
Drug Interaction
3 (.35%)
General Physical Health Deteriorati...
3 (.35%)
Hepatobiliary Disease
3 (.35%)
Hepatotoxicity
3 (.35%)
Lethargy
3 (.35%)
Liver Disorder
3 (.35%)
Metastasis
3 (.35%)
Oral Candidiasis
3 (.35%)
Pancreatitis
3 (.35%)
Pancreatitis Chronic
3 (.35%)
Pyonephrosis
3 (.35%)
Renal Colic
3 (.35%)
Renal Tubular Disorder
3 (.35%)
Respiratory Distress
3 (.35%)
Respiratory Failure
3 (.35%)
Therapeutic Response Decreased
3 (.35%)
Tongue Disorder
3 (.35%)
Tuberculosis
3 (.35%)
Vomiting
3 (.35%)
Adverse Drug Reaction
2 (.23%)
Alanine Aminotransferase Increased
2 (.23%)
Bacterial Sepsis
2 (.23%)
Bleeding Varicose Vein
2 (.23%)
Blood Alkaline Phosphatase Increase...
2 (.23%)
Blood Bilirubin Increased
2 (.23%)
Blood Triglycerides Increased
2 (.23%)
Candida Serology Positive
2 (.23%)
Cardiac Arrest
2 (.23%)
Cd4 Lymphocytes Increased
2 (.23%)

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

What are the most common Indinivir Sulfate adverse events reported to the FDA?

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

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

Hiv Infection
221
Antiretroviral Therapy
19
Drug Use For Unknown Indication
11
Drug Exposure During Pregnancy
8
Product Used For Unknown Indication
6
Systemic Antiviral Treatment
4
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Prophylaxis Against Diarrhoea
3
Hiv Test Positive
3
Maternal Exposure Timing Unspecifie...
2
Acquired Immunodeficiency Syndrome
2
Retroviral Infection
2
Antiviral Prophylaxis
1
Cd4 Lymphocytes Decreased
1
Pneumocystis Jiroveci Infection
1
Hiv Infection Cdc Category A1
1
Hiv Infection Cdc Category A3
1

Indinivir Sulfate Case Reports

What Indinivir Sulfate 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 Indinivir Sulfate. 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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