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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125932431 | 12593243 | 1 | I | 201510 | 20160503 | 20160726 | 20160726 | PER | US-ABBVIE-16P-163-1623490-00 | ABBVIE | 32.33 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125932431 | 12593243 | 1 | PS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | UNKNOWN | 21402 | 125 | UG | TABLET | QD | ||||||
125932431 | 12593243 | 2 | C | IMURAN | AZATHIOPRINE | 1 | 0 | ||||||||||||
125932431 | 12593243 | 3 | C | MULTIVITAMIN | VITAMINS | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125932431 | 12593243 | 1 | Hypothyroidism |
125932431 | 12593243 | 2 | Product used for unknown indication |
125932431 | 12593243 | 3 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125932431 | 12593243 | Drug ineffective | |
125932431 | 12593243 | Fatigue | |
125932431 | 12593243 | Insomnia | |
125932431 | 12593243 | Lethargy | |
125932431 | 12593243 | 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 |
---|---|---|---|---|---|---|
125932431 | 12593243 | 1 | 2009 | 0 |