The Safety Rates Drug Report

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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
117820922 11782092 2 F 20160713 20151126 20160720 PER US-BRISTOL-MYERS SQUIBB COMPANY-BMS-2015-081280 BRISTOL MYERS SQUIBB 0.00 F Y 0.00000 20160720 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
117820922 11782092 1 PS ABILIFY ARIPIPRAZOLE 1 Unknown 5 MG, UNK U 21436 5 MG TABLET
117820922 11782092 2 C EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Unknown U 0
117820922 11782092 3 C TOPAMAX TOPIRAMATE 1 Unknown U 0
117820922 11782092 4 C VALIUM DIAZEPAM 1 Unknown U 0
117820922 11782092 5 C ESGIC ACETAMINOPHENBUTALBITALCAFFEINE 1 U 0
117820922 11782092 6 C HYDROCHLOROTHIAZIDE. HYDROCHLOROTHIAZIDE 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117820922 11782092 1 Depression
117820922 11782092 2 Product used for unknown indication
117820922 11782092 3 Migraine
117820922 11782092 4 Anxiety
117820922 11782092 5 Migraine
117820922 11782092 6 Blood pressure measurement

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
117820922 11782092 Withdrawal syndrome
117820922 11782092 Wrong technique in product usage process

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

no results found

Therapies reported

no results found