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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480013 | 8644441 | I | 8480013-3 | 20110701 | 20120622 | 20120629 | EXP | GB-ABBOTT-12P-167-0948938-00 | ABBOTT | 52 | YR | F | Y | 20120629 | OT | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8480013 | 1020133952 | C | LEVOTHYROXINE SODIUM | 1 | |||||||
| 8480013 | 1020133951 | PS | HUMIRA | 1 | SUBCUTANEOUS | ||||||
| 8480013 | 1020133953 | C | NAPROXEN | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8480013 | 1020133952 | PRODUCT USED FOR UNKNOWN INDICATION |
| 8480013 | 1020133951 | ANKYLOSING SPONDYLITIS |
| 8480013 | 1020133953 | PRODUCT USED FOR UNKNOWN INDICATION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8480013 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8480013 | DEPRESSED MOOD |
| 8480013 | FATIGUE |
| 8480013 | MORBID THOUGHTS |
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 |
|---|---|---|---|---|---|
| 8480013 | 1020133951 | 20110525 | 20120316 |