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
127853341 12785334 1 I 20160922 20160927 20160927 PER PHEH2016US024402 NOVARTIS 0.00 F Y 0.00000 20160927 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
127853341 12785334 1 PS RECLAST ZOLEDRONIC ACID 1 Unknown D 21817 SOLUTION FOR INJECTION
127853341 12785334 2 C SPIRIVA TIOTROPIUM BROMIDE MONOHYDRATE 1 Unknown U 0
127853341 12785334 3 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 Unknown U 0
127853341 12785334 4 C ALBUTEROL. ALBUTEROL 1 Unknown U 0
127853341 12785334 5 C Fish Oil FISH OIL 1 Unknown U 0
127853341 12785334 6 C Calcium CALCIUM 1 Unknown U 0
127853341 12785334 7 C VITAMIN D CHOLECALCIFEROL 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127853341 12785334 1 Product used for unknown indication
127853341 12785334 2 Product used for unknown indication
127853341 12785334 3 Product used for unknown indication
127853341 12785334 4 Product used for unknown indication
127853341 12785334 5 Product used for unknown indication
127853341 12785334 6 Product used for unknown indication
127853341 12785334 7 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127853341 12785334 Muscle tightness
127853341 12785334 Pain in extremity

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found