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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126458701 | 12645870 | 1 | I | 20160419 | 20160429 | 20160811 | 20160811 | PER | US-ENDO PHARMACEUTICALS INC.-2016-003061 | ENDO | 86.00 | YR | F | Y | 65.38000 | KG | 20160811 | CN | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126458701 | 12645870 | 1 | PS | PREDNISONE TABLETS | PREDNISONE | 1 | Unknown | U | 40256 | UNKNOWN | |||||||||
126458701 | 12645870 | 2 | SS | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | U | 78414 | UNKNOWN | |||||||||
126458701 | 12645870 | 3 | SS | WAL FEX 24 HOUR ALLERGY | FEXOFENADINE HYDROCHLORIDE | 1 | Unknown | Y | 0 | TABLETS | |||||||||
126458701 | 12645870 | 4 | SS | WAL FEX 24 HOUR ALLERGY | FEXOFENADINE HYDROCHLORIDE | 1 | Unknown | Y | 0 | TABLETS | |||||||||
126458701 | 12645870 | 5 | SS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | U | 0 | 20 | MG | UNKNOWN | |||||||
126458701 | 12645870 | 6 | SS | XANAX | ALPRAZOLAM | 1 | Unknown | U | 0 | UNKNOWN | |||||||||
126458701 | 12645870 | 7 | SS | PAXIL | PAROXETINE HYDROCHLORIDE | 1 | Unknown | U | 0 | UNKNOWN | |||||||||
126458701 | 12645870 | 8 | SS | ALBUTEROL. | ALBUTEROL | 1 | Unknown | U | 0 | UNKNOWN | |||||||||
126458701 | 12645870 | 9 | SS | ANASTROZOLE. | ANASTROZOLE | 1 | Unknown | U | 0 | UNKNOWN | |||||||||
126458701 | 12645870 | 10 | SS | VITAMIN D3 | CHOLECALCIFEROL | 1 | Unknown | U | 0 | UNKNOWN |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126458701 | 12645870 | 1 | Product used for unknown indication |
126458701 | 12645870 | 2 | Blood pressure management |
126458701 | 12645870 | 3 | Product used for unknown indication |
126458701 | 12645870 | 5 | Gastric disorder |
126458701 | 12645870 | 6 | Product used for unknown indication |
126458701 | 12645870 | 7 | Product used for unknown indication |
126458701 | 12645870 | 8 | Dyspnoea |
126458701 | 12645870 | 9 | Breast cancer |
126458701 | 12645870 | 10 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126458701 | 12645870 | Drug interaction | |
126458701 | 12645870 | Product quality issue | |
126458701 | 12645870 | Somnolence |
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 |
---|---|---|---|---|---|---|
126458701 | 12645870 | 3 | 20160419 | 20160419 | 0 |