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
126278661 12627866 1 I 20160323 20160803 20160806 20160806 EXP CO-ABBVIE-16P-036-1694278-00 ABBVIE 30.30 YR F Y 63.30000 KG 20160805 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
126278661 12627866 1 PS ZEMPLAR PARICALCITOL 1 Intravenous (not otherwise specified) POST DIALYSIS UNKNOWN 20819 5 UG SOLUTION FOR INJECTION
126278661 12627866 2 C CLONIDINE. CLONIDINE 1 0 Q8H
126278661 12627866 3 C NIFEDIPINE. NIFEDIPINE 1 0 Q8H

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126278661 12627866 1 Hyperparathyroidism secondary
126278661 12627866 2 Product used for unknown indication
126278661 12627866 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126278661 12627866 DE
126278661 12627866 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126278661 12627866 Agitation
126278661 12627866 Disorientation
126278661 12627866 Drug dispensing error
126278661 12627866 Rash generalised
126278661 12627866 Sepsis

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
126278661 12627866 1 20141031 20160323 0