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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016638 | 8240712 | F | 8016638-9 | 20111018 | 20111209 | 20111231 | PER | US-ROXANE LABORATORIES, INC.-2011-RO-01493RO | ROXANE LABORATORIES, INC. | 63 | YR | F | Y | 20111231 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 8016638 | 1018419966 | PS | MYCOPHENOLATE MOFETIL | 1 | ORAL | 2000 MG | NR | 065413 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 8016638 | 1018419966 | CHORIORETINOPATHY |
Outcome of event
| no results found |
Reactions reported
| Event ID | PT |
|---|---|
| 8016638 | PRODUCT CONTAMINATION PHYSICAL |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |