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
121239764 12123976 4 F 2016 20160916 20160229 20160922 PER US-PFIZER INC-2016113029 PFIZER 60.00 YR M Y 0.00000 20160922 MD 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
121239764 12123976 1 PS GABAPENTIN. GABAPENTIN 1 Oral 300 MG, 1X/DAY AT BEDTIME Y K0614 20235 300 MG CAPSULE, HARD QD
121239764 12123976 2 SS GABAPENTIN. GABAPENTIN 1 Oral 300 MG, 2X/DAY Y 20235 300 MG CAPSULE, HARD BID
121239764 12123976 3 SS GABAPENTIN. GABAPENTIN 1 Oral 300 MG, 3X/DAY Y 20235 300 MG CAPSULE, HARD TID
121239764 12123976 4 C FENTANYL. FENTANYL 1 UNK 0
121239764 12123976 5 C MORPHINE MORPHINE 1 UNK 0
121239764 12123976 6 C LEXAPRO ESCITALOPRAM OXALATE 1 UNK 0
121239764 12123976 7 C PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 UNK 0
121239764 12123976 8 C TAMSULOSIN TAMSULOSIN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
121239764 12123976 1 Neck injury

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
121239764 12123976 Drug hypersensitivity
121239764 12123976 Irritability
121239764 12123976 Product use issue
121239764 12123976 Somnolence

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
121239764 12123976 1 201601 0
121239764 12123976 3 2016 0