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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125565041 | 12556504 | 1 | I | 20160706 | 20160714 | 20160714 | EXP | CN-WARNER CHILCOTT, LLC-1055047 | WARNER CHILCOTT | JOURNAL: SPINE J?AUTHOR: WANG W, DUAN K, WEI Q, WU Q, LIU J, HAO D?TITLE: SEVERE VERTEBRA COLLAPSE DUE TO VERTEBRA OSTEONESCROSIS AFTER PERCUTANEOUS VERTEBROPLASTY?VOLUME: 16(2) YEAR: 2016 PAGES: E13-E14 | 70.00 | YR | F | Y | 0.00000 | 20160714 | OT | CN | CN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125565041 | 12556504 | 1 | PS | ACTONEL | RISEDRONATE SODIUM | 1 | Oral | U | 20835 | 5 | MG |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125565041 | 12556504 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125565041 | 12556504 | Back pain | |
125565041 | 12556504 | Kyphoscoliosis | |
125565041 | 12556504 | Osteonecrosis | |
125565041 | 12556504 | Spinal compression fracture |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |