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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4430571 | 4168451 | F | 1 | 4430571-0 | 20030101 | 20040803 | 20040818 | EXP | THYR-10185 | GENZYME CORPORATION | 76 | YR | F | N | 20040816 | MD | 20030101 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4430571 | 1005132463 | PS | THYROGEN | 1 | 0.9 MG QD IM | D | D | 20898 | |||
| 4430571 | 1005147310 | SS | THYROGEN | 1 | 0.9 MG QD IM | D | D |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4430571 | 1005132463 | DIAGNOSTIC PROCEDURE |
| 4430571 | 1005147310 | DIAGNOSTIC PROCEDURE |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4430571 | DE |
| 4430571 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4430571 | ANTI-THYROID ANTIBODY POSITIVE |
| 4430571 | COMPUTERISED TOMOGRAM ABNORMAL |
| 4430571 | HYPOCALCAEMIA |
| 4430571 | THYROGLOBULIN INCREASED |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4430571 | CR |
| 4430571 | FGN |
| 4430571 | HP |
| 4430571 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4430571 | 1005132463 | 20010801 | 20010801 | ||
| 4430571 | 1005147310 | 20020101 | 20020101 |