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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125929921 | 12592992 | 1 | I | 201507 | 20150824 | 20160726 | 20160726 | PER | US-ABBVIE-15P-163-1451616-00 | ABBVIE | 50.73 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125929921 | 12592992 | 1 | PS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | TAKE ONE TABLET DAILY SUNDAY THROUGH THURSDAY | 1033772 | 21402 | TABLET | ||||||||
125929921 | 12592992 | 2 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | TAKE 1 TABLET DAILY ON FRIDAY AND SATURDAY | UNKNOWN | 21402 | TABLET | ||||||||
125929921 | 12592992 | 3 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125929921 | 12592992 | 1 | Hypothyroidism |
125929921 | 12592992 | 2 | Hypothyroidism |
125929921 | 12592992 | 3 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125929921 | 12592992 | Fatigue | |
125929921 | 12592992 | Mobility decreased | |
125929921 | 12592992 | Product quality issue | |
125929921 | 12592992 | Sluggishness |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |