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
107443845 10744384 5 F 2010 20160803 20150128 20160808 EXP US-PFIZER INC-2015037276 PFIZER 52.00 YR M Y 0.00000 20160808 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
107443845 10744384 1 PS LYRICA PREGABALIN 1 Oral 100 MG, UNK 21446 100 MG
107443845 10744384 2 SS LYRICA PREGABALIN 1 Oral 200 MG 3 TIMES A DAY AND 50 MG ONCE AT NIGHT 21446 650 MG
107443845 10744384 3 SS LYRICA PREGABALIN 1 Oral 50 MG, 1X/DAY (QHS) 21446 50 MG QD
107443845 10744384 4 C SOMA CARISOPRODOL 1 UNK UNK, 3X/DAY 0 TID
107443845 10744384 5 C LORTAB ACETAMINOPHENHYDROCODONE BITARTRATE 1 [HYDROCODONE BITARTRATE 10MG/ PARACETAMOL 325MG], 3X/DAY 0 1 DF TABLET TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
107443845 10744384 1 Burning sensation
107443845 10744384 2 Paraesthesia
107443845 10744384 3 Neuropathy peripheral

Outcome of event

Event ID CASEID OUTC COD
107443845 10744384 HO
107443845 10744384 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
107443845 10744384 Burning sensation
107443845 10744384 Hernia
107443845 10744384 Malaise
107443845 10744384 Overdose

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
107443845 10744384 2 2010 0