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
127175071 12717507 1 I 20151223 20160125 20160906 20160906 PER US-AMNEAL PHARMACEUTICALS-2016AMN00056 AMNEAL 0.00 F Y 0.00000 20160906 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
127175071 12717507 1 PS GABAPENTIN. GABAPENTIN 1 100 MG, 3X/DAY 78428 100 MG CAPSULE TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127175071 12717507 1 Neuropathy peripheral

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127175071 12717507 Diarrhoea
127175071 12717507 Drug ineffective
127175071 12717507 Oedema peripheral
127175071 12717507 Polyuria
127175071 12717507 Weight increased

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

no results found

Therapies reported

no results found