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
127274181 12727418 1 I 20160712 20160902 20160909 20160909 EXP IE-HPRA-2016-027600 PHFR2016IE007147 NOVARTIS 77.59 YR M Y 0.00000 20160909 OT IE IE

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
127274181 12727418 1 PS ZOMETA ZOLEDRONIC ACID 1 Unknown INFUSION OVER 15/20 MINUTES Y U 21223 SOLUTION FOR INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127274181 12727418 1 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127274181 12727418 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127274181 12727418 Arthralgia
127274181 12727418 Asthenia
127274181 12727418 Back pain
127274181 12727418 Bone pain
127274181 12727418 Decreased appetite
127274181 12727418 Eye pain
127274181 12727418 Fatigue
127274181 12727418 Headache
127274181 12727418 Muscle spasms
127274181 12727418 Nausea
127274181 12727418 Peripheral coldness
127274181 12727418 Photophobia
127274181 12727418 Pyrexia
127274181 12727418 Vision blurred

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
127274181 12727418 1 20160711 0