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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125437781 | 12543778 | 1 | I | 0 | 20160708 | 20160708 | DIR | 87.00 | YR | F | N | 160.00000 | LBS | 20160707 | N | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125437781 | 12543778 | 1 | PS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | 1 PILL | Y | 20160628 | 0 | 150 | ML | PILLULES | QD | ||||
| 125437781 | 12543778 | 3 | C | LUTEIN | LUTEIN | 1 | 0 | ||||||||||||
| 125437781 | 12543778 | 5 | C | FISH OIL | FISH OIL | 1 | 0 | ||||||||||||
| 125437781 | 12543778 | 7 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125437781 | 12543778 | 1 | Hypothyroidism |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125437781 | 12543778 | DS |
| 125437781 | 12543778 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125437781 | 12543778 | Asthenia | |
| 125437781 | 12543778 | Drug ineffective | |
| 125437781 | 12543778 | Fatigue | |
| 125437781 | 12543778 | Sluggishness |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |