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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124080462 | 12408046 | 2 | F | 20160704 | 20160526 | 20160711 | EXP | TR-MLMSERVICE-20160512-0281356-1 | TR-STRIDES ARCOLAB LIMITED-2016SP003561 | STRIDES | 0.00 | Y | 0.00000 | 20160711 | OT | GB | TR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124080462 | 12408046 | 1 | SS | TACROLIMUS. | TACROLIMUS | 1 | UNK | 0 | |||||||||||
| 124080462 | 12408046 | 2 | PS | MYCOPHENOLATE MOFETIL. | MYCOPHENOLATE MOFETIL | 1 | UNK | 90055 | |||||||||||
| 124080462 | 12408046 | 3 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | UNK | 0 | |||||||||||
| 124080462 | 12408046 | 4 | SS | PREDNISOLONE. | PREDNISOLONE | 1 | 20 MG, QD | 0 | 20 | MG | |||||||||
| 124080462 | 12408046 | 5 | SS | METHOTREXATE. | METHOTREXATE | 1 | 7.5 MG, QD | 0 | 7.5 | MG | |||||||||
| 124080462 | 12408046 | 6 | SS | COLCHICINE. | COLCHICINE | 1 | UNK | 0 | |||||||||||
| 124080462 | 12408046 | 7 | C | CALCIUM FOLINATE | LEUCOVORIN CALCIUM | 1 | 50 MG/DAY | 0 | 50 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124080462 | 12408046 | 1 | Immunosuppression |
| 124080462 | 12408046 | 2 | Immunosuppression |
| 124080462 | 12408046 | 3 | Immunosuppression |
| 124080462 | 12408046 | 5 | Rheumatoid arthritis |
| 124080462 | 12408046 | 6 | Immunosuppression |
| 124080462 | 12408046 | 7 | Toxicity to various agents |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124080462 | 12408046 | OT |
| 124080462 | 12408046 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124080462 | 12408046 | Abdominal tenderness | |
| 124080462 | 12408046 | Aphthous ulcer | |
| 124080462 | 12408046 | Asthenia | |
| 124080462 | 12408046 | Atelectasis | |
| 124080462 | 12408046 | Colitis | |
| 124080462 | 12408046 | Delirium | |
| 124080462 | 12408046 | Emphysema | |
| 124080462 | 12408046 | Faeces discoloured | |
| 124080462 | 12408046 | Herpes simplex | |
| 124080462 | 12408046 | Hypotension | |
| 124080462 | 12408046 | Ileus | |
| 124080462 | 12408046 | Metabolic acidosis | |
| 124080462 | 12408046 | Nausea | |
| 124080462 | 12408046 | Necrotising colitis | |
| 124080462 | 12408046 | Neutropenia | |
| 124080462 | 12408046 | Oropharyngeal pain | |
| 124080462 | 12408046 | Pain | |
| 124080462 | 12408046 | Purpura | |
| 124080462 | 12408046 | Pyrexia | |
| 124080462 | 12408046 | Rash | |
| 124080462 | 12408046 | Respiratory distress | |
| 124080462 | 12408046 | Septic shock | |
| 124080462 | 12408046 | Stenotrophomonas infection | |
| 124080462 | 12408046 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |