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
127419301 12741930 1 I 20160906 0 20160913 20160913 DIR US-FDA-350505 FDA-CTU 35.00 YR F N 63.00000 KG 20160913 N 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
127419301 12741930 1 PS CYMBALTA DULOXETINE HYDROCHLORIDE 1 Oral N N 0 QD
127419301 12741930 3 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127419301 12741930 1 Anxiety
127419301 12741930 1 Fibromyalgia

Outcome of event

Event ID CASEID OUTC COD
127419301 12741930 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127419301 12741930 Abdominal pain
127419301 12741930 Aggression
127419301 12741930 Anxiety
127419301 12741930 Chest discomfort
127419301 12741930 Contusion
127419301 12741930 Dyspnoea
127419301 12741930 Economic problem
127419301 12741930 Headache
127419301 12741930 Mood swings
127419301 12741930 Product quality issue
127419301 12741930 Pruritus
127419301 12741930 Vertigo
127419301 12741930 Withdrawal syndrome

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
127419301 12741930 1 20140901 20160906 0