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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7790055 | 8164158 | I | 7790055-9 | 20110524 | 20110930 | PER | US-ASTRAZENECA-2011SE32427 | AZPRODUW00 | 62 | YR | F | Y | 20110930 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|
7790055 | 1017680800 | PS | ARIMIDEX | 1 | ORAL | 020541 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | PT |
---|---|
7790055 | ALOPECIA |
7790055 | INTERVERTEBRAL DISC PROTRUSION |
7790055 | MUSCULOSKELETAL STIFFNESS |
7790055 | ARTHRALGIA |
7790055 | BONE PAIN |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |