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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125284991 | 12528499 | 1 | I | 2007 | 20160627 | 20160705 | 20160705 | EXP | US-ABBVIE-16P-163-1667641-00 | ABBVIE | 0.00 | F | Y | 0.00000 | 20160705 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125284991 | 12528499 | 1 | PS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | UNKNOWN | 21402 | TABLET | QD | ||||||||
| 125284991 | 12528499 | 2 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | ONE TABLET 3 DAYS A WEEK AND 75 MCG TABLETS 4 DAYS A WEEK | UNKNOWN | 21402 | TABLET | ||||||||
| 125284991 | 12528499 | 3 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | ONE TABLET 5 DAYS A WEEK AND 75MCG TABLET 2 DAYS A WEEK K | UNKNOWN | 21402 | TABLET | ||||||||
| 125284991 | 12528499 | 4 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | 1 TABLET 3 DAYS A WEEK AND 50MCG TABLET 4 DAYS A WEEK | Y | UNKNOWN | 21402 | TABLET | |||||||
| 125284991 | 12528499 | 5 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | 75MCG TABLET 2 DAYS A WEEK AND 50MCG TABLET 5 DAYS A WEEK | Y | UNKNOWN | 21402 | TABLET | |||||||
| 125284991 | 12528499 | 6 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | ONE TABLET FOR 6 DAYS AND 1/2 TABLET ONE DAY | Y | UNKNOWN,UNKNOWN,UNKNOWN | 21402 | TABLET | |||||||
| 125284991 | 12528499 | 7 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | Y | UNKNOWN,UNKNOWN,UNKNOWN | 21402 | TABLET | QD | |||||||
| 125284991 | 12528499 | 8 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | ONE TABLET FOR 5 DAYS AND 1/2 TABLET FOR 2 DAYS | Y | UNKNOWN,UNKNOWN,UNKNOWN | 21402 | TABLET |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125284991 | 12528499 | 1 | Hypothyroidism |
| 125284991 | 12528499 | 4 | Hypothyroidism |
| 125284991 | 12528499 | 6 | Hypothyroidism |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125284991 | 12528499 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125284991 | 12528499 | Balance disorder | |
| 125284991 | 12528499 | Blood thyroid stimulating hormone abnormal | |
| 125284991 | 12528499 | C-reactive protein increased | |
| 125284991 | 12528499 | Fatigue | |
| 125284991 | 12528499 | Feeling abnormal | |
| 125284991 | 12528499 | Hodgkin's disease | |
| 125284991 | 12528499 | Injection site infection | |
| 125284991 | 12528499 | Red blood cell sedimentation rate increased | |
| 125284991 | 12528499 | Tremor |
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 |
|---|---|---|---|---|---|---|
| 125284991 | 12528499 | 1 | 20160519 | 20160613 | 0 | |
| 125284991 | 12528499 | 2 | 20160613 | 20160627 | 0 | |
| 125284991 | 12528499 | 3 | 20160627 | 0 | ||
| 125284991 | 12528499 | 4 | 20160613 | 20160627 | 0 | |
| 125284991 | 12528499 | 5 | 20160627 | 0 | ||
| 125284991 | 12528499 | 6 | 201511 | 0 | ||
| 125284991 | 12528499 | 7 | 201511 | 20160323 | 0 | |
| 125284991 | 12528499 | 8 | 20160323 | 20160519 | 0 |