Arthritis, Rheumatoid
Conditions
Brief summary
Study to assess the safety profile of meloxicam by comparing incidence of gastrointestinal adverse events of meloxicam with that of NSAID in the routine daily therapeutic situation.
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients with Indications according to the package insert of the prescribed NSAID
Exclusion criteria
* There is no exclusion criterion, because this Post Marketing Study is an observational study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence for adverse event of gastrointestinal disorder | up to 6 months |
Secondary
| Measure | Time frame |
|---|---|
| Incidence for adverse drug reaction of gastrointestinal disorder | up to 6 months |
| Incidence of adverse events | up to 6 months |
| Incidence of adverse drug reactions | up to 6 months |
| Incidence of serious adverse events | up to 6 months |
| Incidence for adverse events Perforation, Ulcer and Bleeding (PUB) in the upper gastrointestinal tract | up to 6 months |