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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125309143 | 12530914 | 3 | F | 20160704 | 20160706 | 20160713 | EXP | PHHY2016SE092435 | SANDOZ | 29.00 | YR | F | Y | 0.00000 | 20160713 | OT | SE | SE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125309143 | 12530914 | 1 | PS | DICLOFENAC | DICLOFENAC | 1 | Unknown | UNK | U | 74376 | |||||||||
| 125309143 | 12530914 | 2 | I | ESOMEPRAZOLE | ESOMEPRAZOLE | 1 | Unknown | UNK | U | 0 | |||||||||
| 125309143 | 12530914 | 3 | SS | LEVAXIN | LEVOTHYROXINE SODIUM | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125309143 | 12530914 | 1 | Product used for unknown indication |
| 125309143 | 12530914 | 2 | Product used for unknown indication |
| 125309143 | 12530914 | 3 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125309143 | 12530914 | DS |
| 125309143 | 12530914 | HO |
| 125309143 | 12530914 | OT |
| 125309143 | 12530914 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125309143 | 12530914 | Abdominal discomfort | |
| 125309143 | 12530914 | Drug ineffective | |
| 125309143 | 12530914 | Inhibitory drug interaction |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |