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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126673621 | 12667362 | 1 | I | 20160729 | 20160819 | 20160819 | PER | US-PFIZER INC-2016368624 | PFIZER | 0.00 | F | Y | 0.00000 | 20160819 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126673621 | 12667362 | 1 | PS | LEVOTHYROXINE SODIUM. | LEVOTHYROXINE SODIUM | 1 | 112 UG, 1X/DAY(112 MCG, TABLET, ONCE A DAY RESPECTIVELY) | Y | 21301 | 112 | UG | TABLET | QD | ||||||
| 126673621 | 12667362 | 2 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 112 UG, 1X/DAY(112 MCG, TABLET, ONCE A DAY RESPECTIVELY) | Y | 0 | 112 | UG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126673621 | 12667362 | 1 | Autoimmune thyroiditis |
| 126673621 | 12667362 | 2 | Autoimmune thyroiditis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126673621 | 12667362 | Blister | |
| 126673621 | 12667362 | Drug hypersensitivity | |
| 126673621 | 12667362 | Lip blister | |
| 126673621 | 12667362 | Oral mucosal blistering |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |