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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 6733440 | 7394055 | I | 6733440-6 | 20090101 | 20100513 | 20100520 | EXP | US-KINGPHARMUSA00001-K201000590 | KINGPHARMUSA00001 | 53 | YR | F | Y | 40.363 | KG | 20100520 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 6733440 | 1013719558 | PS | LEVOXYL | 1 | 175 MCG, QD | 021301 | |||||
| 6733440 | 1013719559 | SS | LEVOXYL | 1 | 225 MCG, QD | 021301 | |||||
| 6733440 | 1013719560 | SS | LEVOXYL | 1 | 175 MCG, QD | 021301 | |||||
| 6733440 | 1013719561 | C | PREDNISONE TAB | 1 | |||||||
| 6733440 | 1013719562 | C | NEURONTIN | 1 | |||||||
| 6733440 | 1013719563 | C | ATRIPLA | 1 | |||||||
| 6733440 | 1013719564 | C | FLUDROCORTISONE | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 6733440 | 1013719558 | HYPOTHYROIDISM |
| 6733440 | 1013719563 | HIV ANTIBODY |
| 6733440 | 1013719564 | ADRENAL DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 6733440 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 6733440 | DIARRHOEA |
| 6733440 | GASTRIC HYPERMOTILITY |
| 6733440 | HOSPITALISATION |
| 6733440 | THYROXINE DECREASED |
| 6733440 | WEIGHT DECREASED |
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 |
|---|---|---|---|---|---|
| 6733440 | 1013719558 | 19920101 | 20090101 | ||
| 6733440 | 1013719559 | 20090101 | 20100511 | ||
| 6733440 | 1013719560 | 20100515 |