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
126731731 12673173 1 I 20160811 20160808 20160822 20160822 EXP US-ALKERMES INC.-ALK-2016-002167 ALKERMES 58.41 YR M Y 0.00000 20160822 CN 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
126731731 12673173 1 PS VIVITROL NALTREXONE 1 Intramuscular 380 MG, QMO 21897 380 MG INJECTION
126731731 12673173 2 SS NEURONTIN GABAPENTIN 1 1 DF, UNK U 0 1 DF
126731731 12673173 3 C OTHER THERAPEUTIC PRODUCTS (Blood ) 2 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126731731 12673173 1 Alcoholism
126731731 12673173 2 Pain

Outcome of event

Event ID CASEID OUTC COD
126731731 12673173 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126731731 12673173 Drug hypersensitivity
126731731 12673173 Injection site pain
126731731 12673173 Injection site reaction
126731731 12673173 Pain
126731731 12673173 Surgery

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
126731731 12673173 1 20160714 0