Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Oseltamivir
Drug ID BADD_D01627
Description Oseltamivir (marketed as the product TamifluⓇ), is an antiviral neuraminidase inhibitor used for the treatment and prophylaxis of infection with influenza viruses A (including pandemic H1N1) and B. Oseltamivir exerts its antiviral activity by inhibiting the activity of the viral neuraminidase enzyme found on the surface of the virus, which prevents budding from the host cell, viral replication, and infectivity. The clinical benefit of use of oseltamivir is greatest when administered within 48 hours of the onset of influenza symptoms since effectiveness decreases significantly after that point in time; there is generally no benefit in use beyond 48 hours for healthy, low-risk individuals as influenza is a self-limiting illness.[A180574, L7267, A180580] However, antiviral treatment might be beneficial when initiated after 48 hours for patients with severe, complicated or progressive illness or for hospitalized patients.[A180583] According to the CDC, data from clinical trials and observational studies have demonstrated that early antiviral treatment can shorten the duration of fever and illness symptoms, and may reduce the risk of some complications (including pneumonia and respiratory failure). They recommend the use of oseltamivir in people with a higher risk of developing complications including children younger than 2 years, people over 65 years, people with some chronic conditions or immunosuppression, pregnant women, residents of long term care facilities, and indigenous communities for example.[L7264] The benefits of oseltamivir use are controversial; a 2014 Cochrane Review of the evidence found that oseltamivir treatment had limited benefit. The authors concluded that oseltamivir use in healthy adults had small, non-specific effects on symptoms (where the time to first alleviation of symptoms was only reduced from 7 to 6.3 days), it had no effect on hospitalizations, and that there was no evidence for any reductions in complications of influenza such as pneumonia.[A179962, A179965, A179968] Due to the risk of adverse effects such as nausea, vomiting, psychiatric effects and renal adverse events in adults and vomiting in children, the harms are generally considered to outweigh the small clinical benefit of use of oseltamivir. Notably, in 2017, the World Health Organization downgraded oseltamivir from its essential medicines list from a "core" drug to a "complementary" drug, due to limited cost-effectiveness.[A179086] Yearly vaccination with the influenza vaccine is still considered the best preventative measure.
Indications and Usage Oseltamivir (Tamiflu) is for the treatment of uncomplicated acute illness due to influenza infection in patients 1 year and older who have been symptomatic for no more than 2 days. It is also used for the prophylaxis of influenza in adult patients and adolescents 13 years and older.
Marketing Status Prescription; Discontinued
ATC Code J05AH02
DrugBank ID DB00198
KEGG ID D08306
MeSH ID D053139
PubChem ID 65028
TTD Drug ID D0O5NK
NDC Product Code 69238-1266; 46708-414; 62332-413; 42291-664; 42291-666; 50090-4650; 69238-1264; 69238-1265; 62332-415; 46708-413; 46708-415; 62332-414
Synonyms Oseltamivir | GS 4104 | GS4104 | GS-4104 | Tamiflu | GS 4071 | GS4071 | GS-4071
Chemical Information
Molecular Formula C16H28N2O4
CAS Registry Number 196618-13-0
SMILES CCC(CC)OC1C=C(CC(C1NC(=O)C)N)C(=O)OCC
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Arrhythmia02.03.02.0010.000361%Not Available
Arthralgia15.01.02.001--
Ascites09.01.05.003; 07.07.01.001; 02.05.04.002--
Aspartate aminotransferase increased13.03.01.0060.000361%
Aspiration22.02.07.0070.000038%
Asthenia08.01.01.001--Not Available
Asthma22.03.01.002; 10.01.03.0100.000361%Not Available
Atrial fibrillation02.03.03.002--
Atrial septal defect02.04.02.009; 03.07.02.0020.001012%Not Available
Back pain15.03.04.005--
Blindness06.02.02.001; 17.17.01.0030.000361%Not Available
Blindness transient17.17.01.004; 06.02.02.0020.000217%Not Available
Blister23.03.01.001; 12.01.06.0020.000361%Not Available
Blood bilirubin increased13.03.01.0080.000217%
Blood creatine phosphokinase increased13.04.01.0010.000723%
Blood creatinine abnormal13.13.01.0020.000145%Not Available
Blood creatinine increased13.13.01.004--
Blood glucose increased13.02.02.002--Not Available
Blood lactate dehydrogenase increased13.04.02.0020.000145%
Blood pressure decreased13.14.03.0020.000434%Not Available
Blood pressure increased13.14.03.005--Not Available
Blood urea increased13.13.01.0060.000145%Not Available
Body temperature decreased13.15.01.0100.000217%Not Available
Body temperature increased13.15.01.001--Not Available
Bone disorder15.02.04.004--Not Available
Bradycardia02.03.02.0020.000578%Not Available
Bronchiectasis22.03.02.0050.000217%Not Available
Bronchitis22.07.01.001; 11.01.09.001--
Bruxism19.11.03.001; 07.01.06.0080.000145%Not Available
Burning sensation17.02.06.001; 08.01.09.029--Not Available
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