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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125957431 | 12595743 | 1 | I | 20160608 | 20160712 | 20160727 | 20160727 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-120842 | RANBAXY | 83.00 | YR | F | Y | 50.00000 | KG | 20160727 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125957431 | 12595743 | 1 | SS | ELIQUIS | APIXABAN | 1 | Oral | 2.5 MG, BID | 3475 | MG | Y | U | 0 | 2.5 | MG | Q12H | |||
125957431 | 12595743 | 2 | SS | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | Oral | 20 MG, QD | 1360 | MG | U | U | 0 | 20 | MG | ||||
125957431 | 12595743 | 3 | PS | NAPROXEN. | NAPROXEN | 1 | Oral | 500 MG, BID | 292000 | MG | Y | U | 91183 | 500 | MG | Q12H | |||
125957431 | 12595743 | 4 | C | ATORVASTATIN | ATORVASTATIN | 1 | Unknown | UNK | U | U | 0 | ||||||||
125957431 | 12595743 | 5 | C | DIHYDROCODEINE | DIHYDROCODEINE | 1 | Unknown | UNK | U | U | 0 | ||||||||
125957431 | 12595743 | 6 | C | ENALAPRIL | ENALAPRIL | 1 | Unknown | UNK | U | U | 0 | ||||||||
125957431 | 12595743 | 7 | C | GALANTAMINE. | GALANTAMINE | 1 | Unknown | UNK | U | U | 0 | ||||||||
125957431 | 12595743 | 8 | C | PARACETAMOL | ACETAMINOPHEN | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125957431 | 12595743 | 1 | Atrial fibrillation |
125957431 | 12595743 | 2 | Depression |
125957431 | 12595743 | 3 | Arthralgia |
125957431 | 12595743 | 4 | Product used for unknown indication |
125957431 | 12595743 | 5 | Product used for unknown indication |
125957431 | 12595743 | 6 | Product used for unknown indication |
125957431 | 12595743 | 7 | Product used for unknown indication |
125957431 | 12595743 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125957431 | 12595743 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125957431 | 12595743 | 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 |
---|---|---|---|---|---|---|
125957431 | 12595743 | 1 | 20140714 | 20160608 | 0 | |
125957431 | 12595743 | 2 | 20160401 | 20160608 | 0 | |
125957431 | 12595743 | 3 | 20150821 | 20160608 | 0 |