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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125931021 | 12593102 | 1 | I | 201603 | 20160407 | 20160726 | 20160726 | PER | US-ABBVIE-16P-163-1606965-00 | ABBVIE | 49.46 | YR | F | Y | 67.65000 | KG | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125931021 | 12593102 | 1 | PS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | UNKNOWN | 21402 | 100 | UG | TABLET | QD | ||||||
| 125931021 | 12593102 | 2 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | INCREASED TO 2 TABLETS IN A.M. | UNKNOWN | 21402 | 200 | UG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125931021 | 12593102 | 1 | Hypothyroidism |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125931021 | 12593102 | Drug ineffective | |
| 125931021 | 12593102 | Fatigue | |
| 125931021 | 12593102 | Headache | |
| 125931021 | 12593102 | Hypersomnia | |
| 125931021 | 12593102 | Therapy change | |
| 125931021 | 12593102 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 125931021 | 12593102 | 1 | 2014 | 201603 | 0 | |
| 125931021 | 12593102 | 2 | 201603 | 0 |