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
125858971 12585897 1 I 20160322 20160328 20160725 20160725 EXP US-CIPLA LTD.-2016US07101 CIPLA 0.00 Y 0.00000 20160725 CN IN 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
125858971 12585897 1 PS ZONISAMIDE. ZONISAMIDE 1 Oral 100 MG, SINGLE Y 77869 100 MG CAPSULE
125858971 12585897 2 C GABAPENTIN. GABAPENTIN 1 Unknown 300 MG, TID U U 0 300 MG CAPSULE
125858971 12585897 3 C DILAUDID HYDROMORPHONE HYDROCHLORIDE 1 Unknown 2 MG, UNK U U 0 2 MG
125858971 12585897 4 C LYRICA PREGABALIN 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125858971 12585897 2 Neuropathy peripheral
125858971 12585897 3 Pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125858971 12585897 Abdominal discomfort
125858971 12585897 Diarrhoea
125858971 12585897 Erythema
125858971 12585897 Feeling hot
125858971 12585897 Feeling of body temperature change
125858971 12585897 Muscle spasms
125858971 12585897 Nausea
125858971 12585897 Pruritus generalised
125858971 12585897 Skin burning sensation

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
125858971 12585897 1 20160322 20160322 0