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
125996801 12599680 1 I 20150821 20160727 20160727 PER US-SA-2015SA128017 AVENTIS 0.00 A F Y 0.00000 20160727 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
125996801 12599680 1 PS AMBIEN ZOLPIDEM TARTRATE 1 Unknown U UNKNOWN 19908
125996801 12599680 2 SS GABAPENTIN. GABAPENTIN 1 Unknown U UNKNOWN 0 100 MG
125996801 12599680 3 C NORCO ACETAMINOPHENHYDROCODONE BITARTRATE 1 Unknown 0
125996801 12599680 4 C TRIAMTERENE. TRIAMTERENE 1 Unknown 0
125996801 12599680 5 C ARIMIDEX ANASTROZOLE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125996801 12599680 2 Neuralgia

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125996801 12599680 Drug dose omission
125996801 12599680 Dry eye
125996801 12599680 Eye swelling
125996801 12599680 Headache
125996801 12599680 Product use issue
125996801 12599680 Sleep disorder
125996801 12599680 Thirst

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

no results found

Therapies reported

no results found