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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124878033 | 12487803 | 3 | F | 1998 | 20160726 | 20160622 | 20160802 | EXP | PHEH2016US015147 | NOVARTIS | 0.00 | F | Y | 145.00000 | KG | 20160802 | MD | US | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
124878033 | 12487803 | 1 | PS | VIVELLE-DOT | ESTRADIOL | 1 | Transdermal | 0.1 MG, UNK | 20538 | .1 | MG | TRANS-THERAPEUTIC-SYSTEM | |||||||
124878033 | 12487803 | 2 | SS | VIVELLE-DOT | ESTRADIOL | 1 | Transdermal | 0.1 MG, QOD | 20538 | .1 | MG | TRANS-THERAPEUTIC-SYSTEM | |||||||
124878033 | 12487803 | 3 | SS | COPAXONE | GLATIRAMER ACETATE | 1 | Unknown | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
124878033 | 12487803 | 1 | Hormone replacement therapy |
124878033 | 12487803 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
124878033 | 12487803 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
124878033 | 12487803 | Abdominal distension | |
124878033 | 12487803 | Asthma | |
124878033 | 12487803 | Bladder disorder | |
124878033 | 12487803 | Choking | |
124878033 | 12487803 | Drug ineffective | |
124878033 | 12487803 | Dyspnoea | |
124878033 | 12487803 | Haemorrhage | |
124878033 | 12487803 | Migraine | |
124878033 | 12487803 | Multiple sclerosis relapse | |
124878033 | 12487803 | Visual impairment |
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 |
---|---|---|---|---|---|---|
124878033 | 12487803 | 1 | 1997 | 0 |