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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125519851 | 12551985 | 1 | I | 201408 | 0 | 20160712 | 20160712 | DIR | 75.79 | YR | F | N | 122.00000 | LBS | 20160620 | Y | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125519851 | 12551985 | 1 | PS | LEVOXYL | LEVOTHYROXINE SODIUM | 1 | Y | 15N09 | 201611 | 0 | 75 | UG | QD | ||||||
| 125519851 | 12551985 | 2 | SS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 0 | ||||||||||||
| 125519851 | 12551985 | 4 | C | CITRACAL + CALTRATE | 2 | 0 | |||||||||||||
| 125519851 | 12551985 | 5 | C | CENTRUM SILVER | MINERALSVITAMINS | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125519851 | 12551985 | 1 | Autoimmune thyroiditis |
| 125519851 | 12551985 | 1 | Therapy change |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125519851 | 12551985 | Chills | |
| 125519851 | 12551985 | Feeling cold | |
| 125519851 | 12551985 | Nail discolouration | |
| 125519851 | 12551985 | Product measured potency issue |
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 |
|---|---|---|---|---|---|---|
| 125519851 | 12551985 | 1 | 201501 | 201601 | 0 |