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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126456271 | 12645627 | 1 | I | 20160114 | 20160808 | 20160811 | 20160811 | EXP | FR-SA-2016SA146233 | AVENTIS | 73.00 | YR | E | F | Y | 0.00000 | 20160811 | OT | FR | FR |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126456271 | 12645627 | 1 | PS | APROVEL | IRBESARTAN | 1 | Oral | U | UNK | 20757 | 75 | MG | QD | ||||||
126456271 | 12645627 | 2 | SS | IMOVANE | ZOPICLONE | 1 | Unknown | FILM COATED DIVISIBLE TABLET | U | UNK | 0 | 1 | DF | QD | |||||
126456271 | 12645627 | 3 | SS | AMLOR | AMLODIPINE BESYLATE | 1 | Unknown | U | UNK | 0 | 1 | DF | CAPSULE | BID | |||||
126456271 | 12645627 | 4 | SS | XARELTO | RIVAROXABAN | 1 | Oral | Y | UNK | 0 | 1 | DF | FILM-COATED TABLET | QD | |||||
126456271 | 12645627 | 5 | SS | LEXOMIL | BROMAZEPAM | 1 | Unknown | U | UNK | 0 | .5 | DF | QD | ||||||
126456271 | 12645627 | 6 | SS | DIFFU K | POTASSIUM CHLORIDE | 1 | Unknown | U | UNK | 0 | 1 | DF | CAPSULE | QD | |||||
126456271 | 12645627 | 7 | SS | DISCOTRINE | NITROGLYCERIN | 1 | Unknown | U | UNK | 0 | 1 | DF | QD | ||||||
126456271 | 12645627 | 8 | C | CERIS | TROSPIUM CHLORIDE | 1 | 1 AT NOON | 0 | 1 | DF | TABLET | QD | |||||||
126456271 | 12645627 | 9 | C | LASILIX | FUROSEMIDE | 1 | 1 AT NOON | 0 | 20 | MG | QD | ||||||||
126456271 | 12645627 | 10 | C | DEROXAT | PAROXETINE HYDROCHLORIDE | 1 | 0 | 20 | MG | QD |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126456271 | 12645627 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126456271 | 12645627 | Subdural haematoma |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |