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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126362971 | 12636297 | 1 | I | 2012 | 20160727 | 20160809 | 20160809 | EXP | BE-MLMSERVICE-20160721-0358575-8 | BE-STRIDES ARCOLAB LIMITED-2016SP011074 | STRIDES | 0.00 | Y | 0.00000 | 20160809 | OT | GB | BE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126362971 | 12636297 | 1 | PS | MYCOPHENOLATE MOFETIL. | MYCOPHENOLATE MOFETIL | 1 | UNK | U | U | 90055 | |||||||||
| 126362971 | 12636297 | 2 | SS | MYCOPHENOLATE MOFETIL. | MYCOPHENOLATE MOFETIL | 1 | 500 MG, BID | U | U | 90055 | 500 | MG | |||||||
| 126362971 | 12636297 | 3 | SS | TACROLIMUS. | TACROLIMUS | 1 | UNK | U | U | 0 | |||||||||
| 126362971 | 12636297 | 4 | SS | TACROLIMUS. | TACROLIMUS | 1 | 0.5 MG, BID | U | U | 0 | .5 | MG | |||||||
| 126362971 | 12636297 | 5 | SS | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | Intravenous (not otherwise specified) | UNK | 0 | ||||||||||
| 126362971 | 12636297 | 6 | SS | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | 4 MG, PER DAY | 0 | 4 | MG | |||||||||
| 126362971 | 12636297 | 7 | SS | METHYLPREDNISOLONE. | METHYLPREDNISOLONE | 1 | Intravenous (not otherwise specified) | 500 MG, UNK | 0 | 500 | MG | ||||||||
| 126362971 | 12636297 | 8 | SS | POSACONAZOLE | POSACONAZOLE | 1 | Oral | 400 MG, BID | 0 | 400 | MG | ||||||||
| 126362971 | 12636297 | 9 | C | COTRIMOXAZOLE | SULFAMETHOXAZOLETRIMETHOPRIM | 1 | Oral | SULFAMETHOXAZOLE 400MG, TRIMETHOPRIM 80MG | 0 | ||||||||||
| 126362971 | 12636297 | 10 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Oral | 500 MG, BID | 0 | 500 | MG | ||||||||
| 126362971 | 12636297 | 11 | C | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | Oral | 500 MG, BID | 0 | 500 | MG | ||||||||
| 126362971 | 12636297 | 12 | C | IMMUNOGLOBULINS | HUMAN IMMUNOGLOBULIN G | 1 | Intravenous (not otherwise specified) | 2 G/KG | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126362971 | 12636297 | 1 | Immunosuppression |
| 126362971 | 12636297 | 3 | Immunosuppression |
| 126362971 | 12636297 | 5 | Immunosuppression |
| 126362971 | 12636297 | 6 | Transplant rejection |
| 126362971 | 12636297 | 8 | Aspergilloma |
| 126362971 | 12636297 | 9 | Pseudomonas infection |
| 126362971 | 12636297 | 10 | Glucose tolerance impaired |
| 126362971 | 12636297 | 11 | Sinusitis bacterial |
| 126362971 | 12636297 | 12 | Transplant rejection |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126362971 | 12636297 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126362971 | 12636297 | Inappropriate antidiuretic hormone secretion |
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 |
|---|---|---|---|---|---|---|
| 126362971 | 12636297 | 7 | 2012 | 0 | ||
| 126362971 | 12636297 | 8 | 2012 | 2012 | 0 |