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Safety extension study of Phase 3 Osteoarthritis trials with Tanezumab
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Number of Participants With Treatment Emergent Adverse Events (AEs) And Serious Adverse Events (SAEs)
Timeframe: A4091016: Baseline (Day 1) up to 112 days after last dose of study medication (up to Week 80)
Number of Participants With Abnormal Laboratory Findings
Timeframe: A4091016: Day 1 up to Week 80
Number of Participants With Clinically Significant Abnormal Electrocardiogram (ECG) Findings
Timeframe: A4091016: Baseline (Day 1) up to Week 80