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
127878151 12787815 1 I 20160921 20160928 20160928 EXP PHEH2016US024235 NOVARTIS 0.00 F Y 0.00000 20160928 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
127878151 12787815 1 PS RECLAST ZOLEDRONIC ACID 1 Unknown UNK D 21817
127878151 12787815 2 C VITAMIN D CHOLECALCIFEROL 1 Unknown UNK U 0
127878151 12787815 3 C BIOTIN BIOTIN 1 UNK U 0
127878151 12787815 4 C PROTONIX//OMEPRAZOLE OMEPRAZOLE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127878151 12787815 1 Product used for unknown indication
127878151 12787815 2 Product used for unknown indication
127878151 12787815 3 Product used for unknown indication
127878151 12787815 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127878151 12787815 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127878151 12787815 Disturbance in attention
127878151 12787815 Feeling abnormal
127878151 12787815 Gait disturbance
127878151 12787815 Muscle spasms
127878151 12787815 Neck pain
127878151 12787815 Pain in extremity
127878151 12787815 Peripheral swelling

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
127878151 12787815 1 20160916 0