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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 109113102 | 10911310 | 2 | F | 20150227 | 20150313 | 20160720 | EXP | SE-MYLANLABS-2015M1007151 | MYLAN | 0.00 | Y | 0.00000 | 20160720 | CN | SE | SE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 109113102 | 10911310 | 1 | PS | METHOTREXATE. | METHOTREXATE | 1 | UNK | N | 81235 | ||||||||||
| 109113102 | 10911310 | 2 | C | AMLODIPINE BESILATE | AMLODIPINE BESYLATE | 1 | U | 0 | |||||||||||
| 109113102 | 10911310 | 3 | C | MINERALS NOS | MINERALS | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 109113102 | 10911310 | 1 | Crohn's disease |
| 109113102 | 10911310 | 2 | Product used for unknown indication |
| 109113102 | 10911310 | 3 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 109113102 | 10911310 | Arthralgia | |
| 109113102 | 10911310 | Off label use | |
| 109113102 | 10911310 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |