The Safety Rates Drug Report

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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
125290431 12529043 1 I 20160417 20160701 20160705 20160705 EXP CO-ABBVIE-16P-036-1668376-00 ABBVIE 51.28 YR F Y 62.00000 KG 20160705 CN COUNTRY NOT SPECIFIED CO

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
125290431 12529043 1 PS ZEMPLAR PARICALCITOL 1 Intravenous (not otherwise specified) POST DIALYSIS UNKNOWN 20819 5 UG INJECTION
125290431 12529043 2 C FOLIC ACID. FOLIC ACID 1 0
125290431 12529043 3 C CALCIUM CARBONATE. CALCIUM CARBONATE 1 0
125290431 12529043 4 C CAPTOPRIL. CAPTOPRIL 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125290431 12529043 1 Hyperparathyroidism secondary
125290431 12529043 2 Product used for unknown indication
125290431 12529043 3 Product used for unknown indication
125290431 12529043 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125290431 12529043 DE

Reactions reported

Event ID CASEID DRUG REC ACT PT
125290431 12529043 Cardio-respiratory arrest
125290431 12529043 Chest pain

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
125290431 12529043 1 20131101 20151221 0