Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125756181 | 12575618 | 1 | I | 20160707 | 20160720 | 20160720 | EXP | TR-WARNER CHILCOTT, LLC-1055296 | WARNER CHILCOTT | JOURNAL: OSTEOPOROS INT?AUTHOR: UGURLAR M?TITLE: ALENDRONATE- AND RISEDRONATE-INDUCED ACUTE POLYARTHRITIS?VOLUME: EPUB YEAR: 2016 PAGES: EPUB | 52.00 | YR | F | Y | 0.00000 | 20160720 | OT | TR | TR |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125756181 | 12575618 | 1 | PS | ACTONEL | RISEDRONATE SODIUM | 1 | Oral | 20835 | 35 | MG | |||||||||
| 125756181 | 12575618 | 2 | SS | ALENDRONATE | ALENDRONATE SODIUM | 1 | Oral | 0 | 70 | MG |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125756181 | 12575618 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125756181 | 12575618 | Arthralgia | |
| 125756181 | 12575618 | Joint effusion | |
| 125756181 | 12575618 | Joint range of motion decreased | |
| 125756181 | 12575618 | Joint swelling | |
| 125756181 | 12575618 | Joint warmth | |
| 125756181 | 12575618 | Myalgia | |
| 125756181 | 12575618 | Polyarthritis | |
| 125756181 | 12575618 | Synovitis |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |