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
125828991 12582899 1 I 20150902 20160708 20160722 20160722 EXP AU-PFIZER INC-2016346971 PFIZER 49.00 YR F Y 0.00000 20160722 OT AU AU

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
125828991 12582899 1 PS MORPHINE SULFATE. MORPHINE SULFATE 1 U 19999
125828991 12582899 2 SS FORTEO TERIPARATIDE 1 UNK UNK, 1X/DAY U 0 1 DF QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125828991 12582899 2 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
125828991 12582899 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125828991 12582899 Arthralgia
125828991 12582899 Cardiac flutter
125828991 12582899 Chest discomfort
125828991 12582899 Concomitant disease aggravated
125828991 12582899 Cough
125828991 12582899 Fatigue
125828991 12582899 Injection site pain
125828991 12582899 Insomnia
125828991 12582899 Nausea
125828991 12582899 Pain
125828991 12582899 Polyp
125828991 12582899 Serum ferritin decreased

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
125828991 12582899 2 20150731 0