Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8480320 | 8644626 | I | 8480320-4 | 20120529 | 20120630 | PER | US-ASTRAZENECA-2012SE34538 | AZPRODUW00 | YR | Y | 20120630 | CN | UNITED STATES |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
8480320 | 1020135205 | PS | NEXIUM | 1 | ORAL | 021153 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
8480320 | OSTEOPOROSIS |
8480320 | MULTIPLE FRACTURES |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |