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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125932091 | 12593209 | 1 | I | 201605 | 20160520 | 20160726 | 20160726 | PER | US-ABBVIE-16P-163-1633742-00 | ABBVIE | 61.95 | YR | F | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125932091 | 12593209 | 1 | PS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | 1048491 | 21402 | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125932091 | 12593209 | 1 | Hypothyroidism |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125932091 | 12593209 | Abdominal distension | |
125932091 | 12593209 | Asthenia | |
125932091 | 12593209 | Disorientation | |
125932091 | 12593209 | Dizziness | |
125932091 | 12593209 | Fatigue | |
125932091 | 12593209 | Product quality issue | |
125932091 | 12593209 | 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 |
---|---|---|---|---|---|---|
125932091 | 12593209 | 1 | 1986 | 0 |