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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126397221 | 12639722 | 1 | I | 20160729 | 20160810 | 20160810 | EXP | AU-ALVOGEN-2016-ALVOGEN-027331-01 | AU-ALVOGEN-2016-ALVOGEN-027331 | ALVOGEN | 0.00 | M | Y | 0.00000 | 20160810 | OT | AU | AU |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126397221 | 12639722 | 1 | PS | NIFEDIPINE. | NIFEDIPINE | 1 | U | 20198 | |||||||||||
126397221 | 12639722 | 2 | SS | ATENOLOL. | ATENOLOL | 1 | U | 0 | |||||||||||
126397221 | 12639722 | 3 | SS | ENALAPRIL MALEATE. | ENALAPRIL MALEATE | 1 | U | 0 | |||||||||||
126397221 | 12639722 | 4 | SS | ALLOPURINOL. | ALLOPURINOL | 1 | U | 0 | |||||||||||
126397221 | 12639722 | 5 | SS | MYLANTA | ALUMINUM HYDROXIDEDIMETHICONEMAGNESIUM HYDROXIDE | 1 | U | 0 | |||||||||||
126397221 | 12639722 | 6 | SS | COLCHICINE. | COLCHICINE | 1 | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126397221 | 12639722 | 1 | Product used for unknown indication |
126397221 | 12639722 | 2 | Product used for unknown indication |
126397221 | 12639722 | 3 | Product used for unknown indication |
126397221 | 12639722 | 4 | Product used for unknown indication |
126397221 | 12639722 | 5 | Product used for unknown indication |
126397221 | 12639722 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126397221 | 12639722 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126397221 | 12639722 | Renal impairment |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |