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
125996811 12599681 1 I 20150803 20150825 20160727 20160727 PER US-SA-2015SA134083 AVENTIS 47.00 YR 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
125996811 12599681 1 I OXYBUTYNIN HYDROCHLORIDE OXYBUTYNIN CHLORIDE 1 Unknown U UNK 0
125996811 12599681 2 PS AMBIEN ZOLPIDEM TARTRATE 1 Unknown U UNK 19908
125996811 12599681 3 I LEUPROLIDE ACETATE. LEUPROLIDE ACETATE 1 Intramuscular 1037527 0 3.75 MG INJECTION
125996811 12599681 4 I SINGULAIR MONTELUKAST SODIUM 1 Unknown U UNK 0
125996811 12599681 5 I SIMVASTATIN. SIMVASTATIN 1 Unknown U UNK 0
125996811 12599681 6 I OXYCODONE HYDROCHLORIDE. OXYCODONE HYDROCHLORIDE 1 Unknown U UNK 0
125996811 12599681 7 SS TRAMADOL. TRAMADOL 1 Unknown U UNK 0
125996811 12599681 8 SS DETROL TOLTERODINE TARTRATE 1 Unknown U UNK 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125996811 12599681 Asthenia
125996811 12599681 Confusional state
125996811 12599681 Decreased appetite
125996811 12599681 Dizziness
125996811 12599681 Drug interaction
125996811 12599681 Dry mouth
125996811 12599681 Insomnia
125996811 12599681 Micturition disorder
125996811 12599681 Weight decreased

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
125996811 12599681 3 201505 0