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
108552697 10855269 7 F 20160715 20150223 20160715 EXP US-PFIZER INC-2015064496 PFIZER 0.00 F Y 0.00000 20160715 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
108552697 10855269 1 PS LYRICA PREGABALIN 1 UNK 21446
108552697 10855269 2 SS EFFEXOR XR VENLAFAXINE HYDROCHLORIDE 1 UNK U 20699 PROLONGED-RELEASE CAPSULE
108552697 10855269 3 C FENTANYL. FENTANYL 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
108552697 10855269 1 Fibromyalgia

Outcome of event

Event ID CASEID OUTC COD
108552697 10855269 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
108552697 10855269 Cardiac disorder
108552697 10855269 Cardiac failure
108552697 10855269 Depression
108552697 10855269 Drug ineffective
108552697 10855269 Malaise
108552697 10855269 Pain
108552697 10855269 Road traffic accident
108552697 10855269 Visual impairment
108552697 10855269 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
108552697 10855269 1 20151117 0