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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125697483 | 12569748 | 3 | F | 20160804 | 20160719 | 20160811 | EXP | JP-B.I. PHARMACEUTICALS,INC./RIDGEFIELD-2016-BI-46190NB | BOEHRINGER INGELHEIM | YASUDA S,ASANO M,KITADA Y,FUJIOKA K,ANDO D,ISHIDUKA T. A CASE OF IDIOPATHIC HYPOPARAHYROIDISM THAT WAS DIAGNOSED FROM LOSS OF CONSCIOUSNESS. - 2016;. | 68.00 | YR | M | Y | 62.50000 | KG | 20160811 | OT | COUNTRY NOT SPECIFIED | JP |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125697483 | 12569748 | 1 | PS | MICARDIS | TELMISARTAN | 1 | Oral | 40 MG | U | 20850 | 40 | MG | TABLET | QD | |||||
125697483 | 12569748 | 2 | C | KALLIDINOGENASE | KALLIDINOGENASE | 1 | Oral | 150 MG | U | 0 | 50 | MG | TID |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125697483 | 12569748 | 1 | Hypertension |
125697483 | 12569748 | 2 | Hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125697483 | 12569748 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125697483 | 12569748 | Hypoparathyroidism |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |