The Safety Rates Drug Report

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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
125694172 12569417 2 F 20160718 20160719 20160805 PER US-PFIZER INC-2016318186 PFIZER 90.00 YR F Y 0.00000 20160805 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
125694172 12569417 1 PS GABAPENTIN. GABAPENTIN 1 100 MG PILL ONCE OR TWICE A DAY U 20235 100 MG
125694172 12569417 2 SS GABAPENTIN. GABAPENTIN 1 100 MG, UNK U 20235 100 MG
125694172 12569417 3 SS GABAPENTIN. GABAPENTIN 1 300 MG PILLS UP TO 3 PILLS PER DAY U 20235
125694172 12569417 4 C LOSARTAN. LOSARTAN 1 0
125694172 12569417 5 C TRAZODONE TRAZODONE HYDROCHLORIDE 1 UNK 0
125694172 12569417 6 C DOXYCYCLINE. DOXYCYCLINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125694172 12569417 1 Neuropathy peripheral
125694172 12569417 2 Neuralgia
125694172 12569417 3 Pain in extremity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125694172 12569417 Dizziness
125694172 12569417 Drug dose omission
125694172 12569417 Fall
125694172 12569417 Head injury
125694172 12569417 Product use issue
125694172 12569417 Somnolence

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found