The Safety Rates Drug Report

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Drug     Injury     Quarter    

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
125420241 12542024 1 I 20160629 20160707 20160708 20160708 EXP CO-ABBVIE-16P-036-1671686-00 ABBVIE 68.28 YR F Y 0.00000 20160708 OT 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
125420241 12542024 1 PS ZEMPLAR PARICALCITOL 1 Intravenous (not otherwise specified) UNKNOWN 20819 10 UG INJECTION /wk

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125420241 12542024 1 Hyperparathyroidism secondary

Outcome of event

Event ID CASEID OUTC COD
125420241 12542024 DE
125420241 12542024 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125420241 12542024 Blood glucose increased
125420241 12542024 Cardio-respiratory arrest
125420241 12542024 Malaise
125420241 12542024 Pyrexia
125420241 12542024 Respiratory failure
125420241 12542024 Sepsis
125420241 12542024 Septic shock
125420241 12542024 Somnolence
125420241 12542024 Urinary tract infection

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
125420241 12542024 1 20150220 20160704 0