DrugCite
Search

COMBIVIR

Adverse Events
Drug Profile
Learn More
Reference
About Results
Comments

Combivir Adverse Events Reported to the FDA Over Time

How are Combivir adverse event reports trending over time?

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

Most Common Combivir Adverse Events Reported to the FDA

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

Drug Exposure During Pregnancy
1727 (9.68%)
Abortion Spontaneous
389 (2.18%)
Anaemia
319 (1.79%)
Premature Baby
292 (1.64%)
Stillbirth
249 (1.4%)
Pregnancy
212 (1.19%)
Pyrexia
179 (1%)
Abortion Induced
175 (.98%)
Vomiting
143 (.8%)
Diarrhoea
141 (.79%)
Nausea
127 (.71%)
Show More Show More
Cardiac Murmur
112 (.63%)
Abdominal Pain
106 (.59%)
Asthenia
106 (.59%)
Congenital Anomaly
106 (.59%)
Caesarean Section
104 (.58%)
Fatigue
100 (.56%)
Haemoglobin Decreased
99 (.56%)
Maternal Drugs Affecting Foetus
97 (.54%)
Alanine Aminotransferase Increased
94 (.53%)
Ventricular Septal Defect
94 (.53%)
Abdominal Distension
92 (.52%)
Pancytopenia
91 (.51%)
Exomphalos
90 (.5%)
Dyspnoea
88 (.49%)
Hepatitis
87 (.49%)
Neutropenia
87 (.49%)
Sepsis
87 (.49%)
Headache
84 (.47%)
Atrial Septal Defect
81 (.45%)
Cough
81 (.45%)
Intra-uterine Death
81 (.45%)
Ascites
80 (.45%)
Normal Newborn
80 (.45%)
Trisomy 21
77 (.43%)
Cardiac Malposition
74 (.41%)
Live Birth
71 (.4%)
Deformity Thorax
69 (.39%)
Diaphragmatic Aplasia
69 (.39%)
Aspartate Aminotransferase Increase...
67 (.38%)
Jaundice
67 (.38%)
Polydactyly
67 (.38%)
Premature Labour
67 (.38%)
Rash
66 (.37%)
Pallor
65 (.36%)
Pneumonia
65 (.36%)
Blood Bilirubin Increased
63 (.35%)
Cryptorchism
63 (.35%)
Malaise
63 (.35%)
Microcephaly
63 (.35%)
Patent Ductus Arteriosus
63 (.35%)
Hepatic Displacement
62 (.35%)
Talipes
61 (.34%)
Weight Decreased
61 (.34%)
Foetal Growth Retardation
60 (.34%)
Pre-eclampsia
58 (.33%)
Premature Rupture Of Membranes
58 (.33%)
Oedema Peripheral
56 (.31%)
Dizziness
54 (.3%)
Death
53 (.3%)
Pericardial Effusion
53 (.3%)
Pneumothorax
53 (.3%)
Thrombocytopenia
49 (.27%)
Confusional State
48 (.27%)
Respiratory Distress
48 (.27%)
Hydrops Foetalis
47 (.26%)
Hydronephrosis
46 (.26%)
Eating Disorder
45 (.25%)
Blood Alkaline Phosphatase Increase...
44 (.25%)
Blood Lactate Dehydrogenase Increas...
44 (.25%)
Gastroenteritis
44 (.25%)
Loss Of Consciousness
43 (.24%)
Pain In Extremity
43 (.24%)
Ultrasound Antenatal Screen Abnorma...
43 (.24%)
Cardiac Failure
41 (.23%)
Drug Interaction
41 (.23%)
Hepatotoxicity
41 (.23%)
Abdominal Hernia
40 (.22%)
Cardiomyopathy
40 (.22%)
Congenital Central Nervous System A...
40 (.22%)
Dehydration
40 (.22%)
Foetal Disorder
40 (.22%)
Cytolytic Hepatitis
39 (.22%)
Hepatic Enzyme Increased
39 (.22%)
Death Neonatal
38 (.21%)
Disseminated Intravascular Coagulat...
38 (.21%)
Developmental Delay
37 (.21%)
Leukopenia
37 (.21%)
Alpha 1 Foetoprotein Abnormal
36 (.2%)
Abdominal Pain Upper
35 (.2%)
Bone Marrow Failure
35 (.2%)
Heart Disease Congenital
35 (.2%)
Placental Disorder
35 (.2%)
Vanishing Bile Duct Syndrome
35 (.2%)
C-reactive Protein Increased
34 (.19%)
Chest Pain
34 (.19%)
Hepatomegaly
34 (.19%)
Laboratory Test Abnormal
34 (.19%)
Myocardial Infarction
34 (.19%)
Ultrasound Scan Abnormal
34 (.19%)
Spina Bifida
33 (.19%)

ExportShare/Embed GraphExport Export Data

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

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

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

Hiv Infection
3734
Drug Exposure During Pregnancy
371
Antiretroviral Therapy
257
Antiviral Treatment
198
Antiviral Prophylaxis
195
Drug Use For Unknown Indication
180
Show More Show More
Hiv Test Positive
123
Prophylaxis Against Hiv Infection
102
Prophylaxis
101
Acquired Immunodeficiency Syndrome
97
Maternal Exposure Timing Unspecifie...
86
Product Used For Unknown Indication
70
Human Immunodeficiency Virus Transm...
58
Maternal Exposure During Pregnancy
42
Systemic Antiviral Treatment
28
Retroviral Infection
15
Viral Infection
10
Acute Hiv Infection
9
Asymptomatic Hiv Infection
9
Pathogen Resistance
7
Vertical Infection Transmission
7
Ill-defined Disorder
4
Accidental Needle Stick
4
Lentivirus Test Positive
3
Exposure To Communicable Disease
2
Pregnancy
2
Hiv Infection Cdc Category A3
2
Biliary Cirrhosis
1
Pneumocystis Jiroveci Infection
1
Bite
1
Hiv Test
1
Urticaria
1
Herpes Virus Infection
1
Congenital Hiv Infection
1
Accidental Exposure
1
Pancytopenia
1
Sexually Transmitted Disease
1
Chronic Obstructive Pulmonary Disea...
1
Autoimmune Disorder
1
Pneumocystis Carinii Infection
1
Biliary Cirrhosis Primary
1
Local Antiviral Treatment
1
Hiv Infection Cdc Category B2
1
Convulsion Neonatal
1
Castlemans Disease
1
Immunodeficiency
1
End Stage Aids
1
Exposure Via Blood
1
Hiv Antibody Positive
1

Drug Labels

LabelLabelerEffective
CombivirStat Rx USA27-OCT-09
CombivirRebel Distributors Corp24-SEP-10
CombivirPD-Rx Pharmaceuticals, Inc.14-MAR-11
CombivirGlaxoSmithKline LLC14-MAR-11
CombivirHHS/Program Support Center/Supply Service Center03-JAN-12
CombivirH.J. Harkins Company, Inc.02-FEB-12
CombivirViiV Healthcare Company16-JAN-13
CombivirREMEDYREPACK INC. 11-MAR-13
CombivirREMEDYREPACK INC. 23-APR-13
CombivirREMEDYREPACK INC. 23-APR-13
CombivirREMEDYREPACK INC. 23-APR-13

Combivir Case Reports

What Combivir 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 Combivir. 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 Combivir.