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
127362961 12736296 1 I 20160818 20160905 20160912 20160912 EXP GB-MHRA-EYC 00144547 GB-MYLANLABS-2016M1037556 MYLAN 0.00 Y 0.00000 20160912 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
127362961 12736296 1 PS ZOLEDRONIC ACID ZOLEDRONIC ACID 1 Intravenous (not otherwise specified) 1 DF, UNK U 202650 1 DF INTRAVENOUS INFUSION
127362961 12736296 2 C AMITRIPTYLINE AMITRIPTYLINE 1 UNK U 0
127362961 12736296 3 C AMLODIPINE AMLODIPINE BESYLATE 1 UNK U 0
127362961 12736296 4 C COCODAMOL ACETAMINOPHENCODEINE PHOSPHATE 1 UNK U 0
127362961 12736296 5 C COLECALCIFEROL CHOLECALCIFEROL 1 UNK U 0
127362961 12736296 6 C OMEPRAZOLE. OMEPRAZOLE 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127362961 12736296 1 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
127362961 12736296 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127362961 12736296 Atrial fibrillation
127362961 12736296 Chest discomfort
127362961 12736296 Dyspnoea
127362961 12736296 Malaise
127362961 12736296 Palpitations

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
127362961 12736296 1 20160816 20160816 0