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
124738023 12473802 3 F 2016 20160802 20160616 20160802 EXP US-PFIZER INC-2016299372 PFIZER 0.00 M Y 0.00000 20160802 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
124738023 12473802 1 PS GABAPENTIN. GABAPENTIN 1 Oral 100 MG, 3X/DAY U 20235 100 MG CAPSULE, HARD TID
124738023 12473802 2 SS GABAPENTIN. GABAPENTIN 1 U 20235 CAPSULE, HARD
124738023 12473802 3 SS GABAPENTIN. GABAPENTIN 1 U 20235 CAPSULE, HARD
124738023 12473802 4 SS GABAPENTIN. GABAPENTIN 1 U 20235 CAPSULE, HARD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124738023 12473802 1 Hypoaesthesia
124738023 12473802 2 Paraesthesia
124738023 12473802 3 Neuropathy peripheral
124738023 12473802 4 Sciatica

Outcome of event

Event ID CASEID OUTC COD
124738023 12473802 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124738023 12473802 Balance disorder
124738023 12473802 Condition aggravated
124738023 12473802 Coordination abnormal
124738023 12473802 Drug ineffective for unapproved indication
124738023 12473802 Fatigue
124738023 12473802 Insomnia
124738023 12473802 Parkinson's disease
124738023 12473802 Restless legs syndrome
124738023 12473802 Somnolence
124738023 12473802 Tremor

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
124738023 12473802 1 201604 0