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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8626051 | 8732460 | F | 8626051-9 | 20090101 | 20120817 | 20120827 | EXP | US-ABBOTT-12P-163-0967682-00 | ABBOTT | 39 | YR | F | Y | 20120827 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8626051 | 1020680076 | SS | METHOTREXATE | 1 | |||||||
| 8626051 | 1020680085 | C | METHOTREXATE | 1 | |||||||
| 8626051 | 1020680084 | C | HORMONE INJECTIONS | 2 | |||||||
| 8626051 | 1020680074 | SS | HUMIRA | 1 | UNKNOWN | ||||||
| 8626051 | 1020680077 | SS | METHOTREXATE | 1 | |||||||
| 8626051 | 1020680080 | C | ZYRTEC | 1 | |||||||
| 8626051 | 1020680086 | C | PREDNISONE TAB | 1 | |||||||
| 8626051 | 1020680078 | C | BCP | 2 | |||||||
| 8626051 | 1020680079 | C | NASONEX | 1 | |||||||
| 8626051 | 1020680075 | SS | HUMIRA | 1 | UNKNOWN | ||||||
| 8626051 | 1020680081 | C | GENERIC FOR PRILOSEC | 2 | ORAL | DAILY | |||||
| 8626051 | 1020680073 | PS | HUMIRA | 1 | UNKNOWN | ||||||
| 8626051 | 1020680082 | C | ALBUTEROL | 1 | |||||||
| 8626051 | 1020680083 | C | SEMAR | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8626051 | 1020680076 | PRODUCT USED FOR UNKNOWN INDICATION |
| 8626051 | 1020680085 | PRODUCT USED FOR UNKNOWN INDICATION |
| 8626051 | 1020680084 | INFERTILITY |
| 8626051 | 1020680080 | HYPERSENSITIVITY |
| 8626051 | 1020680086 | PRODUCT USED FOR UNKNOWN INDICATION |
| 8626051 | 1020680078 | PRODUCT USED FOR UNKNOWN INDICATION |
| 8626051 | 1020680079 | HYPERSENSITIVITY |
| 8626051 | 1020680081 | PRODUCT USED FOR UNKNOWN INDICATION |
| 8626051 | 1020680073 | RHEUMATOID ARTHRITIS |
| 8626051 | 1020680082 | ASTHMA |
| 8626051 | 1020680083 | OVARIAN DISORDER |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 8626051 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 8626051 | ADVERSE DRUG REACTION |
| 8626051 | JOINT STIFFNESS |
| 8626051 | INCORRECT ROUTE OF DRUG ADMINISTRATION |
| 8626051 | HORMONE LEVEL ABNORMAL |
| 8626051 | WRONG TECHNIQUE IN DRUG USAGE PROCESS |
| 8626051 | BREECH PRESENTATION |
| 8626051 | UMBILICAL CORD AROUND NECK |
| 8626051 | ARTHRALGIA |
| 8626051 | INJECTION SITE HAEMATOMA |
| 8626051 | INFERTILITY |
| 8626051 | LUNG DISORDER |
| 8626051 | INJECTION SITE INDURATION |
| 8626051 | RHEUMATOID ARTHRITIS |
| 8626051 | FALSE POSITIVE INVESTIGATION RESULT |
| 8626051 | PREMATURE RUPTURE OF MEMBRANES |
| 8626051 | AMNIOTIC FLUID VOLUME DECREASED |
| 8626051 | INJECTION SITE PAIN |
| 8626051 | DRUG EFFECT DECREASED |
| 8626051 | MALAISE |
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 |
|---|---|---|---|---|---|
| 8626051 | 1020680074 | 20070801 | 20081201 | ||
| 8626051 | 1020680077 | 20120810 | |||
| 8626051 | 1020680075 | 20090801 | |||
| 8626051 | 1020680073 | 20060101 | 20070101 |