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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126100001 | 12610000 | 1 | I | 20160726 | 20160801 | 20160801 | EXP | GB-MHRA-MIDB-58A4922C-DA19-4D41-A792-960A3D37BD28 | GB-WATSON-2016-16743 | WATSON | 80.00 | YR | F | Y | 0.00000 | 20160801 | CN | GB | GB |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126100001 | 12610000 | 1 | PS | Prednisolone (Unknown) | PREDNISOLONE | 1 | Oral | 10 MG, QAM; EVERY MORNING OM | Y | UNCONFIRMED | 80354 | 10 | MG | UNK | QD | ||||
| 126100001 | 12610000 | 2 | SS | Prednisolone (Unknown) | PREDNISOLONE | 1 | Oral | 15 MG, QAM | Y | UNCONFIRMED | 80354 | 15 | MG | UNK | QD | ||||
| 126100001 | 12610000 | 3 | SS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | UNK | Y | UNCONFIRMED | 0 | UNK | |||||||
| 126100001 | 12610000 | 4 | C | DIHYDROCODEINE | DIHYDROCODEINE | 1 | Oral | 30MG - 60MG THREE TIMES A DAY; AS NECESSARY | U | 0 | TID | ||||||||
| 126100001 | 12610000 | 5 | C | ENOXAPARIN | ENOXAPARIN | 1 | Subcutaneous | UNK; 60MG/0.6ML UNTIL INRWITHIN RANGE | U | 0 | |||||||||
| 126100001 | 12610000 | 6 | C | FENBID | IBUPROFEN | 1 | Topical | UNK | U | 0 | |||||||||
| 126100001 | 12610000 | 7 | C | LANSOPRAZOLE. | LANSOPRAZOLE | 1 | Oral | 30 MG, DAILY | U | 0 | 30 | MG | QD | ||||||
| 126100001 | 12610000 | 8 | C | PARACETAMOL | ACETAMINOPHEN | 1 | Oral | 1 G, QID | U | 0 | 1 | G | |||||||
| 126100001 | 12610000 | 9 | C | WARFARIN | WARFARIN | 1 | Oral | 1 MG, UNK; AS PER INR BOOKLET | U | 0 | 1 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126100001 | 12610000 | 1 | Rheumatoid arthritis |
| 126100001 | 12610000 | 3 | Product used for unknown indication |
| 126100001 | 12610000 | 4 | Product used for unknown indication |
| 126100001 | 12610000 | 5 | Product used for unknown indication |
| 126100001 | 12610000 | 6 | Product used for unknown indication |
| 126100001 | 12610000 | 7 | Product used for unknown indication |
| 126100001 | 12610000 | 8 | Product used for unknown indication |
| 126100001 | 12610000 | 9 | Deep vein thrombosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126100001 | 12610000 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126100001 | 12610000 | Acute kidney injury | |
| 126100001 | 12610000 | International normalised ratio increased | |
| 126100001 | 12610000 | Joint swelling | |
| 126100001 | 12610000 | Peripheral swelling | |
| 126100001 | 12610000 | Polyarthritis |
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 |
|---|---|---|---|---|---|---|
| 126100001 | 12610000 | 1 | 20160520 | 0 |