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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125496381 | 12549638 | 1 | I | 2014 | 20160629 | 20160712 | 20160712 | EXP | US-BAYER-2016-131863 | BAYER | 0.00 | F | Y | 0.00000 | 20160712 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125496381 | 12549638 | 1 | PS | CIPRO | CIPROFLOXACIN HYDROCHLORIDE | 1 | UNK | 21473 | MODIFIED-RELEASE FILM-COATED TABLET | ||||||||||
125496381 | 12549638 | 2 | SS | ZITHROMAX | AZITHROMYCIN DIHYDRATE | 1 | Subcutaneous | UNK | 0 | ||||||||||
125496381 | 12549638 | 3 | C | HUMIRA | ADALIMUMAB | 1 | 40 MG, UNK | 0 | 40 | MG | |||||||||
125496381 | 12549638 | 4 | C | SPIRONOLACTON | SPIRONOLACTONE | 1 | UNK | 0 | |||||||||||
125496381 | 12549638 | 5 | C | CEREBREX | CALCIUM GLYCEROPHOSPHATECALCIUM PHOSPHATEGLUTAMIC ACIDVITAMIN B | 1 | UNK | 0 | |||||||||||
125496381 | 12549638 | 6 | C | FUROSEMIDE. | FUROSEMIDE | 1 | UNK | 0 | |||||||||||
125496381 | 12549638 | 7 | C | IMURAN | AZATHIOPRINE | 1 | UNK | 0 | |||||||||||
125496381 | 12549638 | 8 | C | ATENOLOL. | ATENOLOL | 1 | UNK | 0 | |||||||||||
125496381 | 12549638 | 9 | C | CYMBALTA | DULOXETINE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
125496381 | 12549638 | 10 | C | OSTEO BI-FLEX | CHONDROITIN SULFATE AGLUCOSAMINE | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125496381 | 12549638 | 1 | Bronchitis |
125496381 | 12549638 | 2 | Bronchitis |
125496381 | 12549638 | 3 | Crohn's disease |
125496381 | 12549638 | 4 | Fluid retention |
125496381 | 12549638 | 5 | Osteoarthritis |
125496381 | 12549638 | 6 | Fluid retention |
125496381 | 12549638 | 7 | Crohn's disease |
125496381 | 12549638 | 8 | Hypertension |
125496381 | 12549638 | 9 | Depression |
125496381 | 12549638 | 10 | Osteoarthritis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125496381 | 12549638 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125496381 | 12549638 | Abdominal pain | |
125496381 | 12549638 | Bronchitis | |
125496381 | 12549638 | Candida infection | |
125496381 | 12549638 | Depression | |
125496381 | 12549638 | Diarrhoea | |
125496381 | 12549638 | Dyskinesia | |
125496381 | 12549638 | Gastric ulcer | |
125496381 | 12549638 | Hiatus hernia | |
125496381 | 12549638 | Memory impairment | |
125496381 | 12549638 | Nausea | |
125496381 | 12549638 | Parasomnia | |
125496381 | 12549638 | Product use issue | |
125496381 | 12549638 | Pyrexia | |
125496381 | 12549638 | Rash pruritic | |
125496381 | 12549638 | Sleep disorder |
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 |
---|---|---|---|---|---|---|
125496381 | 12549638 | 1 | 2014 | 2014 | 0 | |
125496381 | 12549638 | 3 | 200809 | 2014 | 0 |