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
127809901 12780990 1 I 20151116 20160916 20160926 20160926 EXP GB-MHRA-EYC 00145212 GB-MYLANLABS-2016M1040194 MYLAN 0.00 Y 0.00000 20160926 MD GB GB

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
127809901 12780990 1 PS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK Y U 202650 5 MG INTRAVENOUS INFUSION
127809901 12780990 2 C CALCICHEW D3 CALCIUMCHOLECALCIFEROL 1 UNK U 0
127809901 12780990 3 C ELLESTE-SOLO 2 UNK U 0
127809901 12780990 4 C FENTANYL. FENTANYL 1 UNK U 0
127809901 12780990 5 C MEBEVERINE MEBEVERINE 1 UNK U 0
127809901 12780990 6 C PARACETAMOL ACETAMINOPHEN 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127809901 12780990 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
127809901 12780990 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127809901 12780990 Malaise
127809901 12780990 Migraine
127809901 12780990 Nausea

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
127809901 12780990 1 20151113 20151113 0