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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126541871 | 12654187 | 1 | I | 20160809 | 0 | 20160815 | 20160815 | DIR | 70.00 | YR | M | N | 240.00000 | LBS | 20160812 | N | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126541871 | 12654187 | 1 | PS | RESTASIS | CYCLOSPORINE | 1 | Ophthalmic | Y | D | 0 | 90 | DF | CAPSULE | BID | |||||
126541871 | 12654187 | 3 | C | ASPIRIN. | ASPIRIN | 1 | 0 | ||||||||||||
126541871 | 12654187 | 5 | C | MUCINEX | GUAIFENESIN | 1 | 0 | ||||||||||||
126541871 | 12654187 | 7 | C | METAMUCIL | PLANTAGO SEED | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126541871 | 12654187 | 1 | Eye disorder |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126541871 | 12654187 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126541871 | 12654187 | Eye irritation |
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 |
---|---|---|---|---|---|---|
126541871 | 12654187 | 1 | 20160808 | 20160810 | 0 |