DFDA

Oseltamivir

Treatment for Lower Respiratory Infections

Typical Dosage: 75 mg twice daily

Effectiveness
75%
Safety Score
65%
Clinical Trials
4
Participants
50K

Comparative Safety Scale(Higher is safer)

Cyanide☠️
MethπŸ’€
Cigarettes🚬
Chemo☒️
Alcohol🍺
MorphineπŸ’Š
AntibioticsπŸ’‰
TylenolπŸ’Š
ExerciseπŸƒ
WaterπŸ’§
65
DangerousModerateSafe
Treatment Details
Dosage Range
75 mg twice daily
Time to Effect
1-2 days
Treatment Duration
5 days
Evidence Quality
HIGH
Number Needed to Treat (NNT)
25(Treat 25 patients to see 1 additional successful outcome)
Number Needed to Harm (NNH)
8(Treat 8 patients to see 1 additional serious adverse event)
Confidence Score
85%confidence in effectiveness data
Health Economics
Annual Cost of Care
Drug Cost:$75
Monitoring:$150
Side Effect Mgmt:$5
Total Annual:$230
Cost-Effectiveness Analysis
Cost-Effectiveness Rating
GOOD
ICER
$75,000/QALY
QALYs Gained
0.03
Outcome-Based Costs
Cost per Responder
$353.85
Cost per Remission
$920
Comparison vs Supportive Care
Cost Difference
+$75/year
More expensive
QALY Difference
+0.03 QALYs
Better outcomes
Dominance
No dominance
Oseltamivir Outcomes

for Lower Respiratory Infections

Efficacy Outcomes
Overall Effectiveness
+75%
Response Rate
+65%
Remission Rate
+25%
Common Side Effects
Nausea/vomiting
+12.5%
Headache
+2.5%
Neuropsychiatric events
+0.05%

WARNING: LIMITED TRIALS AVAILABLE

You can search for trials, but you probably can't join any because the 1% Treaty hasn't passed yet. Most trials are severely limited by lack of funding and bureaucratic barriers. Help change this!

Active Clinical Trials
1 active trial recruiting for Oseltamivir in Lower Respiratory Infections

Intravenous N-acetylcysteine and Oseltamivir Versus Oseltamivir in Adults Hospitalized With Influenza and Pneumonia

NCT03900988RECRUITINGPHASE3
View Study
160 participants
INTERVENTIONAL
Hong Kong, Hong Kong
Started: May 8, 2023
Completed Clinical Trials
1 completed trial for Oseltamivir in Lower Respiratory Infections

Oseltamivir Randomised Controlled Efficacy Trial

NCT00707941COMPLETEDPHASE3
View Study
1.19K participants
INTERVENTIONAL
Dhaka, Bangladesh
Started: May 1, 2008