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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125930351 | 12593035 | 1 | I | 201601 | 20160316 | 20160726 | 20160726 | PER | US-ABBVIE-16P-163-1586076-00 | ABBVIE | 81.62 | YR | M | Y | 0.00000 | 20160726 | CN | US | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125930351 | 12593035 | 1 | PS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | Y | UNKNOWN | 21402 | TABLET | QD | |||||||
| 125930351 | 12593035 | 2 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | UNKNOWN | 21402 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125930351 | 12593035 | 1 | Hypothyroidism |
| 125930351 | 12593035 | 2 | Hypothyroidism |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125930351 | 12593035 | Anxiety | |
| 125930351 | 12593035 | Insomnia | |
| 125930351 | 12593035 | Product quality issue | |
| 125930351 | 12593035 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 125930351 | 12593035 | 1 | 20160306 | 0 | ||
| 125930351 | 12593035 | 2 | 20160309 | 0 |