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
125556391 12555639 1 I 20160107 20160629 20160714 20160714 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-120057 RANBAXY 16.00 YR F Y 0.00000 20160714 OT GB GB

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
125556391 12555639 1 PS VENLAFAXINE VENLAFAXINE HYDROCHLORIDE 1 Oral 150-375 91272
125556391 12555639 2 C DESONIDE. DESONIDE 1 Unknown U U 0
125556391 12555639 3 C FEXOFENADINE HYDROCHLORIDE. FEXOFENADINE HYDROCHLORIDE 1 Unknown U U 0
125556391 12555639 4 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 Unknown U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125556391 12555639 1 Anxiety
125556391 12555639 2 Product used for unknown indication
125556391 12555639 3 Product used for unknown indication
125556391 12555639 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125556391 12555639 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125556391 12555639 Asthenia
125556391 12555639 Dizziness
125556391 12555639 Dry eye
125556391 12555639 Dry mouth
125556391 12555639 Fatigue
125556391 12555639 Hot flush
125556391 12555639 Hypersomnia
125556391 12555639 Muscular weakness
125556391 12555639 Night sweats
125556391 12555639 Thirst

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
125556391 12555639 1 20160105 0