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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126523871 | 12652387 | 1 | I | 20160722 | 20160815 | 20160815 | PER | US-PFIZER INC-2016358393 | PFIZER | 65.00 | YR | F | Y | 72.00000 | KG | 20160815 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126523871 | 12652387 | 1 | PS | LEVOXYL | LEVOTHYROXINE SODIUM | 1 | UNK | U | 21301 | TABLET | |||||||||
126523871 | 12652387 | 2 | SS | LEVOXYL | LEVOTHYROXINE SODIUM | 1 | Oral | 88 UG, 1X/DAY | U | 21301 | 88 | UG | TABLET | QD | |||||
126523871 | 12652387 | 3 | C | NATURE-THROID | THYROID, PORCINE | 1 | Oral | 25 UG, 1X/DAY | 0 | 25 | UG | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126523871 | 12652387 | 1 | Thyroid disorder |
126523871 | 12652387 | 3 | Tri-iodothyronine increased |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126523871 | 12652387 | 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 |
---|---|---|---|---|---|---|
126523871 | 12652387 | 1 | 2014 | 0 | ||
126523871 | 12652387 | 2 | 201606 | 0 |