Person who experienced the adverse event (patient)
| Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5155097 | 6178259 | I | 5155097-0 | 20060804 | 20061120 | DIR | 48 | YR | M | N | 148 | LBS | 20061116 | PH | N | Y | UNITED STATES |
Drug(s) used by person
| Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5155097 | 1007870250 | PS | LITHIUM 300 MG | 2 | ORAL | 900 MG DAILY PO |
Indications of drugs used
| no results found |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 5155097 | HYPOTHYROIDISM |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |