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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126670151 | 12667015 | 1 | I | 20160725 | 20160819 | 20160819 | EXP | IL-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-121762 | RANBAXY | 15.00 | YR | F | Y | 0.00000 | 20160819 | OT | IL | IL |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126670151 | 12667015 | 1 | PS | Isotretinoin | ISOTRETINOIN | 1 | Oral | 40 MG, DAILY | U | 76041 | 40 | MG | |||||||
126670151 | 12667015 | 2 | SS | Isotretinoin | ISOTRETINOIN | 1 | Oral | DAILY DOSE WAS REDUCED | U | 76041 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126670151 | 12667015 | 1 | Ichthyosis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126670151 | 12667015 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126670151 | 12667015 | Blood creatine phosphokinase increased | |
126670151 | 12667015 | Off label use | |
126670151 | 12667015 | Unmasking of previously unidentified disease |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |