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
125723261 12572326 1 I 20150902 20160708 20160719 20160719 EXP AU-NAPPMUNDI-GBR-2016-0038817 PURDUE 48.80 YR F Y 0.00000 20160715 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
125723261 12572326 1 PS MORPHINE SULFATE. MORPHINE SULFATE 1 Unknown UNK U U 74862
125723261 12572326 2 SS Morphine Hydrochloride MORPHINE HYDROCHLORIDE 1 Unknown UNK U U 0 ORAL SOLUTION
125723261 12572326 3 SS FORTEO TERIPARATIDE 1 Unknown AT NIGHT U U 0 INJECTION
125723261 12572326 4 SS FORTEO TERIPARATIDE 1 Unknown ONCE DAILY U U 0 INJECTION

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125723261 12572326 1 Product used for unknown indication
125723261 12572326 2 Product used for unknown indication
125723261 12572326 3 Osteoporosis

Outcome of event

Event ID CASEID OUTC COD
125723261 12572326 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125723261 12572326 Arthralgia
125723261 12572326 Chest discomfort
125723261 12572326 Concomitant disease aggravated
125723261 12572326 Cough
125723261 12572326 Fatigue
125723261 12572326 Injection site pain
125723261 12572326 Insomnia
125723261 12572326 Nausea
125723261 12572326 Pain
125723261 12572326 Polyp
125723261 12572326 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
125723261 12572326 4 20150731 0