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
125250491 12525049 1 I 20160114 20160624 20160704 20160704 EXP GB-MHRA-EYC 00141234 GB-PFIZER INC-2016317389 PFIZER 46.00 YR F Y 65.77000 KG 20160704 OT GB GB

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
125250491 12525049 1 PS NEURONTIN GABAPENTIN 1 Oral 200MG MORNING AND NIGHT, 100MG TEATIME (TITRATED UP SLOWLY THEN DOWN SLOWLY TO STOP) N M64841 20235
125250491 12525049 2 C CODEINE PHOSPHATE CODEINE PHOSPHATE 1 STOPPED AFTER TITRATING UP GABAPENTIN. 0
125250491 12525049 3 C FYBOGEL MEBEVERINE 2 ONLY IN LAST 28 DAYS 0
125250491 12525049 4 C LANSOPRAZOLE. LANSOPRAZOLE 1 RECENTLY STOPPED 0
125250491 12525049 5 C PARACETAMOL ACETAMINOPHEN 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125250491 12525049 1 Intervertebral disc protrusion

Outcome of event

Event ID CASEID OUTC COD
125250491 12525049 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125250491 12525049 Disturbance in attention
125250491 12525049 Dizziness
125250491 12525049 Fatigue
125250491 12525049 Feeling abnormal
125250491 12525049 Flatulence
125250491 12525049 Gastrointestinal motility disorder
125250491 12525049 Memory impairment
125250491 12525049 Speech disorder
125250491 12525049 Visual impairment

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
125250491 12525049 1 20160112 20160508 0