Person who experienced the adverse event (patient)
| Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126713891 | 12671389 | 1 | I | 201607 | 20160808 | 20160822 | 20160822 | EXP | US-SUN PHARMACEUTICAL INDUSTRIES LTD-2016US-122288 | RANBAXY | 61.43 | YR | F | Y | 0.00000 | 20160822 | CN | US | US |
Drug(s) used by person
| Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126713891 | 12671389 | 1 | PS | BACTRIM DS | SULFAMETHOXAZOLETRIMETHOPRIM | 1 | Oral | 1 DF, QD | Y | 17377 | 1 | DF | |||||||
| 126713891 | 12671389 | 2 | SS | BACTRIM DS | SULFAMETHOXAZOLETRIMETHOPRIM | 1 | Oral | 01 DF, QD | U | 17377 | 1 | DF | |||||||
| 126713891 | 12671389 | 3 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | 40 MG, FORTNIGHT | Y | 0 | 40 | MG | SOLUTION FOR INJECTION | ||||||
| 126713891 | 12671389 | 4 | SS | HUMIRA | ADALIMUMAB | 1 | Subcutaneous | 40 MG, FORTNIGHT | Y | 0 | 40 | MG | SOLUTION FOR INJECTION | ||||||
| 126713891 | 12671389 | 5 | C | METHOTREXATE. | METHOTREXATE | 1 | Oral | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126713891 | 12671389 | 1 | Product used for unknown indication |
| 126713891 | 12671389 | 2 | Product used for unknown indication |
| 126713891 | 12671389 | 3 | Rheumatoid arthritis |
| 126713891 | 12671389 | 4 | Rheumatoid arthritis |
| 126713891 | 12671389 | 5 | Rheumatoid arthritis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126713891 | 12671389 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126713891 | 12671389 | Gastric disorder | |
| 126713891 | 12671389 | Inappropriate schedule of drug administration | |
| 126713891 | 12671389 | Urinary tract infection |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|---|
| 126713891 | 12671389 | 1 | 20160709 | 201607 | 0 | |
| 126713891 | 12671389 | 2 | 201607 | 0 | ||
| 126713891 | 12671389 | 3 | 2010 | 0 | ||
| 126713891 | 12671389 | 4 | 201601 | 0 |