LABA/ICS Combination (e.g., Fluticasone/Salmeterol)

Treatment for Copd

Typical Dosage: Fluticasone 250 mcg/Salmeterol 50 mcg twice daily

Effectiveness
75%
Safety Score
50%
Clinical Trials
1
Participants
60K

Comparative Safety Scale(Higher is safer)

Cyanide☠️
Meth💀
Cigarettes🚬
Chemo☢️
Alcohol🍺
Morphine💊
Antibiotics💉
Tylenol💊
Exercise🏃
Water💧
50
DangerousModerateSafe
Treatment Details
Dosage Range
Fluticasone 250 mcg/Salmeterol 50 mcg twice daily
Time to Effect
15-30 minutes (bronchodilation), weeks-months (exacerbation reduction)
Treatment Duration
Lifetime
Evidence Quality
HIGH
Number Needed to Treat (NNT)
10(Treat 10 patients to see 1 additional successful outcome)
Number Needed to Harm (NNH)
15(Treat 15 patients to see 1 additional serious adverse event)
Confidence Score
90%confidence in effectiveness data
Health Economics
Annual Cost of Care
Drug Cost:$3,600
Monitoring:$800
Side Effect Mgmt:$150
Total Annual:$4,550
Cost-Effectiveness Analysis
Cost-Effectiveness Rating
EXCELLENT
ICER
$45,000/QALY
QALYs Gained
0.03
Outcome-Based Costs
Cost per Responder
$7,583
Comparison vs Salmeterol (LABA monotherapy)
Cost Difference
+$300/year
More expensive
QALY Difference
+0.03 QALYs
Better outcomes
Dominance
No dominance
LABA/ICS Combination (e.g., Fluticasone/Salmeterol) Outcomes

for Copd

Efficacy Outcomes
Overall Effectiveness
+75%
Response Rate
+60%
Common Side Effects
Nasopharyngitis
+15%
Headache
+12%
Oral candidiasis
+10%
Pneumonia
+6%
Bronchitis
+5%

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
No active trials currently recruiting for this treatment

No active trials found in ClinicalTrials.gov

Completed Clinical Trials
1 completed trial for LABA/ICS Combination (e.g., Fluticasone/Salmeterol) in Copd

WEUSKOP6416: Evaluating Pneumonia in Chronic Obstructive Pulmonary Disease (COPD) Subjects

NCT01763463COMPLETED
View Study
1 participants
OBSERVATIONAL
Started: Jul 1, 2012