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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126109084 | 12610908 | 4 | F | 201606 | 20160907 | 20160801 | 20160913 | PER | US-PFIZER INC-2016344094 | PFIZER | 62.00 | YR | F | Y | 53.00000 | KG | 20160913 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126109084 | 12610908 | 1 | PS | LEVOXYL | LEVOTHYROXINE SODIUM | 1 | Oral | 75 UG, 2X/DAY | U | 15N07 | 21301 | 75 | UG | TABLET | BID | ||||
126109084 | 12610908 | 2 | SS | LEVOXYL | LEVOTHYROXINE SODIUM | 1 | UNK | U | 21301 | TABLET | |||||||||
126109084 | 12610908 | 3 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | 0.012 MG, DAILY | 0 | .012 | MG |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126109084 | 12610908 | Constipation | |
126109084 | 12610908 | Drug ineffective | |
126109084 | 12610908 | Fatigue | |
126109084 | 12610908 | Feeling abnormal | |
126109084 | 12610908 | Product quality issue |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |