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
126214042 12621404 2 F 20160620 20160822 20160804 20160825 PER US-PFIZER INC-2016372762 PFIZER 53.00 YR F Y 0.00000 20160825 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
126214042 12621404 1 PS GABAPENTIN. GABAPENTIN 1 400 MG, 4X/DAY 20235 400 MG QID
126214042 12621404 2 C SYNTHROID LEVOTHYROXINE SODIUM 1 150 MG, 1X/DAY 0 150 MG QD
126214042 12621404 3 C REMERON MIRTAZAPINE 1 15 MG, 1X/DAY 0 15 MG QD
126214042 12621404 4 C ZANAFLEX TIZANIDINE HYDROCHLORIDE 1 4 MG, 2X/DAY 0 4 MG BID
126214042 12621404 5 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 UNK UNK, 4X/DAY [OXYCODONE HYDROCHLORIDE: 7.5] 0 QID
126214042 12621404 6 C ZANEX 2 1 MG, 3X/DAY 0 1 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126214042 12621404 1 Nerve injury

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126214042 12621404 Abdominal discomfort
126214042 12621404 Malaise
126214042 12621404 Product use issue

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
126214042 12621404 1 2016 201608 0
126214042 12621404 2 1987 0
126214042 12621404 3 2009 0
126214042 12621404 4 2014 0
126214042 12621404 5 2008 0
126214042 12621404 6 2001 0