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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125593171 | 12559317 | 1 | I | 20160706 | 20160715 | 20160715 | EXP | US-PAR PHARMACEUTICAL COMPANIES-2016SCPR015615 | PAR | 0.00 | Y | 0.00000 | 20160715 | CN | COUNTRY NOT SPECIFIED | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125593171 | 12559317 | 1 | PS | Diltiazem HCl | DILTIAZEM HYDROCHLORIDE | 1 | Oral | 1 DF, OD | 74984 | 1 | DF | ||||||||
125593171 | 12559317 | 2 | SS | Diltiazem HCl | DILTIAZEM HYDROCHLORIDE | 1 | Oral | 1 DF, OD | 74984 | 1 | DF | ||||||||
125593171 | 12559317 | 3 | C | CRESTOR | ROSUVASTATIN CALCIUM | 1 | Oral | 1 DF, OD | 0 | 1 | DF | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125593171 | 12559317 | 1 | Arrhythmia |
125593171 | 12559317 | 3 | Blood cholesterol abnormal |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125593171 | 12559317 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125593171 | 12559317 | Drug ineffective for unapproved indication |
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 |
---|---|---|---|---|---|---|
125593171 | 12559317 | 2 | 201605 | 0 |