non-small cell lung cancer
Conditions
Interventions
None listed
Sponsors
Merck Biopharma Co., Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All patients who received at least 1 dose of this drug during the survey period.
Exclusion criteria
Exclusion criteria: None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Investigate occurrence of interstitial lung disease, fluid retention, hepatic function disorder, renal impairment and QT interval prolongation | — |
Countries
Japan
Contacts
Public ContactTatsuya Ogura
Merck Biopharma Co., Ltd. PMS Planning & Strategy
Outcome results
None listed