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
126757631 12675763 1 I 20160407 20160823 20160823 PER US-JAZZ-2016-US-006638 JAZZ 0.00 F Y 0.00000 20160823 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
126757631 12675763 1 PS XYREM SODIUM OXYBATE 1 Oral 2.25 G, BID 21196 2.25 G ORAL SOLUTION
126757631 12675763 2 SS XYREM SODIUM OXYBATE 1 Oral DOSE ADJUSTMENTS 21196 ORAL SOLUTION
126757631 12675763 3 SS XYREM SODIUM OXYBATE 1 Oral 4.5 G, BID 21196 4.5 G ORAL SOLUTION
126757631 12675763 4 SS PROVIGIL MODAFINIL 1 UNK U 0 TABLET
126757631 12675763 5 C FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 U 0
126757631 12675763 6 C CLARITIN LORATADINE 1 U 0
126757631 12675763 7 C NUVIGIL ARMODAFINIL 1 U 0
126757631 12675763 8 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 U 0
126757631 12675763 9 C ZYRTEC CETIRIZINE HYDROCHLORIDE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126757631 12675763 1 Narcolepsy
126757631 12675763 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126757631 12675763 Blood pressure increased
126757631 12675763 Peripheral swelling

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
126757631 12675763 1 201305 201305 0
126757631 12675763 3 201311 0
126757631 12675763 4 20140926 0