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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
116180833 | 11618083 | 3 | F | 20140714 | 20160823 | 20151010 | 20160831 | EXP | FR-SYMPLMED PHARMACEUTICALS-2015SYM00226 | SYMPLMED PHARMACEUTICALS | 0.00 | Y | 0.00000 | 20160831 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
116180833 | 11618083 | 1 | PS | Coversyl | PERINDOPRIL | 1 | Oral | 5 MG, QD | U | U | UNKNOWN | 20184 | 5 | MG | TABLET | ||||
116180833 | 11618083 | 2 | SS | CARDENSIEL | BISOPROLOL FUMARATE | 1 | Oral | 2.5 MG, QD | U | U | UNKNOWN | 0 | 2.5 | MG | |||||
116180833 | 11618083 | 3 | SS | LASILIX /00032601/ | FUROSEMIDE | 1 | Oral | 80 MG, QD | U | U | UNKNOWN | 0 | 80 | MG | |||||
116180833 | 11618083 | 4 | SS | TAHOR | ATORVASTATIN CALCIUM | 1 | Oral | 20 MG, QD | U | U | UNKNOWN | 0 | 20 | MG | |||||
116180833 | 11618083 | 5 | SS | AMLOR | AMLODIPINE BESYLATE | 1 | Oral | 10 MG, QD | U | U | UNKNOWN | 0 | 10 | MG | |||||
116180833 | 11618083 | 6 | SS | PREVISCAN | FLUINDIONE | 1 | Oral | 20 MG, UNK | U | U | UNKNOWN | 0 | 20 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
116180833 | 11618083 | 1 | Product used for unknown indication |
116180833 | 11618083 | 2 | Product used for unknown indication |
116180833 | 11618083 | 3 | Product used for unknown indication |
116180833 | 11618083 | 4 | Product used for unknown indication |
116180833 | 11618083 | 5 | Product used for unknown indication |
116180833 | 11618083 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
116180833 | 11618083 | DE |
116180833 | 11618083 | HO |
116180833 | 11618083 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
116180833 | 11618083 | Atrial fibrillation | |
116180833 | 11618083 | Atrial flutter | |
116180833 | 11618083 | Cardiac failure | |
116180833 | 11618083 | Cardio-respiratory arrest | |
116180833 | 11618083 | Pneumonia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |