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
127754231 12775423 1 I 20151116 20160916 20160923 20160923 EXP GB-MHRA-EYC 00145212 GB-PFIZER INC-2016437690 PFIZER 60.00 YR F Y 58.00000 KG 20160923 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
127754231 12775423 1 PS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 5 MG, UNK Y 90621 5 MG
127754231 12775423 2 C CALCICHEW D3 CALCIUMCHOLECALCIFEROL 1 UNK 0
127754231 12775423 3 C ELLESTE-SOLO 2 UNK 0
127754231 12775423 4 C FENTANYL. FENTANYL 1 UNK 0
127754231 12775423 5 C MEBEVERINE MEBEVERINE 1 UNK 0
127754231 12775423 6 C PARACETAMOL ACETAMINOPHEN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127754231 12775423 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
127754231 12775423 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127754231 12775423 Malaise
127754231 12775423 Migraine
127754231 12775423 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
127754231 12775423 1 20151113 20151113 0