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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121312343 | 12131234 | 3 | F | 201306 | 20160912 | 20160301 | 20160921 | PER | US-JNJFOC-20160203204 | JANSSEN | 65.54 | YR | A | F | Y | 0.00000 | 20160921 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121312343 | 12131234 | 1 | SS | XARELTO | RIVAROXABAN | 1 | Oral | Y | N | UNKNOWN | 0 | 20 | MG | TABLET | QD | ||||
121312343 | 12131234 | 2 | SS | XARELTO | RIVAROXABAN | 1 | Oral | Y | N | UNKNOWN | 0 | 20 | MG | TABLET | QD | ||||
121312343 | 12131234 | 3 | PS | XARELTO | RIVAROXABAN | 1 | Oral | Y | N | UNKNOWN | 202439 | 20 | MG | TABLET | QD | ||||
121312343 | 12131234 | 4 | SS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | U | U | 19012 | UNSPECIFIED | ||||||||
121312343 | 12131234 | 5 | SS | IBUPROFEN. | IBUPROFEN | 1 | Unknown | U | U | 19012 | 800 | MG | UNSPECIFIED | QD | |||||
121312343 | 12131234 | 6 | C | LEVOTHYROXINE. | LEVOTHYROXINE | 1 | Unknown | D | 0 | UNSPECIFIED | |||||||||
121312343 | 12131234 | 7 | C | ENALAPRIL | ENALAPRIL | 1 | Unknown | D | 0 | UNSPECIFIED | |||||||||
121312343 | 12131234 | 8 | C | FISH OIL | FISH OIL | 1 | Unknown | D | 0 | UNSPECIFIED | |||||||||
121312343 | 12131234 | 9 | C | MULTAQ | DRONEDARONE | 1 | Unknown | D | 0 | UNSPECIFIED | |||||||||
121312343 | 12131234 | 10 | C | CARDIZEM | DILTIAZEM HYDROCHLORIDE | 1 | Unknown | D | 0 | UNSPECIFIED | |||||||||
121312343 | 12131234 | 11 | C | ALENDRONATE | ALENDRONATE SODIUM | 1 | Unknown | D | 0 | UNSPECIFIED | |||||||||
121312343 | 12131234 | 12 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | D | 0 | UNSPECIFIED | |||||||||
121312343 | 12131234 | 13 | C | DETROL | TOLTERODINE TARTRATE | 1 | Unknown | D | 0 | UNSPECIFIED |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
121312343 | 12131234 | 1 | Thrombosis prophylaxis |
121312343 | 12131234 | 2 | Cerebrovascular accident prophylaxis |
121312343 | 12131234 | 3 | Atrial fibrillation |
121312343 | 12131234 | 5 | Arthritis |
121312343 | 12131234 | 6 | Product used for unknown indication |
121312343 | 12131234 | 7 | Product used for unknown indication |
121312343 | 12131234 | 8 | Product used for unknown indication |
121312343 | 12131234 | 9 | Product used for unknown indication |
121312343 | 12131234 | 10 | Product used for unknown indication |
121312343 | 12131234 | 11 | Product used for unknown indication |
121312343 | 12131234 | 12 | Product used for unknown indication |
121312343 | 12131234 | 13 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
121312343 | 12131234 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
121312343 | 12131234 | Upper gastrointestinal haemorrhage |
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 |
---|---|---|---|---|---|---|
121312343 | 12131234 | 1 | 20130108 | 20130220 | 0 | |
121312343 | 12131234 | 2 | 20130108 | 20130220 | 0 | |
121312343 | 12131234 | 3 | 20130108 | 20130220 | 0 |