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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6251138 | 7037403 | I | 6251138-8 | 20090205 | 20090403 | 20090630 | PER | US-ABBOTT-09P-163-0566617-00 | ABBOTT LABORATORIES | F | Y | 20090630 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6251138 | 1011814129 | PS | ZEMPLAR | 1 | ORAL | UNKNOWN | 021606 | ||||
| 6251138 | 1011814130 | SS | ZEMPLAR | 1 | ORAL | UNKNOWN | 021606 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6251138 | 1011814129 | HYPERPARATHYROIDISM |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 6251138 | ASTHENIA |
| 6251138 | DIZZINESS |
| 6251138 | FATIGUE |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 6251138 | 1011814129 | 20090102 |