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
124636592 12463659 2 F 20160823 20160614 20160829 EXP US-PFIZER INC-2016283127 PFIZER 61.00 YR F Y 49.00000 KG 20160829 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
124636592 12463659 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, DAILY 21992 50 MG PROLONGED-RELEASE TABLET
124636592 12463659 2 SS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 21992 PROLONGED-RELEASE TABLET
124636592 12463659 3 C BYSTOLIC NEBIVOLOL HYDROCHLORIDE 1 UNKNOWN DOSE (LOW DOSE), 1X/DAY (AT NIGHT) 0 QD
124636592 12463659 4 C LUMIGAN BIMATOPROST 1 Ophthalmic 1 GTT, 1X/DAY (1 DROP IN EACH EYE AT NIGHT) 0 1 GTT EYE DROPS QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124636592 12463659 1 Mood swings
124636592 12463659 2 Attention deficit/hyperactivity disorder
124636592 12463659 3 Blood pressure abnormal
124636592 12463659 4 Glaucoma

Outcome of event

Event ID CASEID OUTC COD
124636592 12463659 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
124636592 12463659 Abdominal pain upper
124636592 12463659 Diarrhoea
124636592 12463659 Drug dose omission
124636592 12463659 Malaise
124636592 12463659 Nausea
124636592 12463659 Nervousness
124636592 12463659 Withdrawal syndrome

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
124636592 12463659 1 2009 0
124636592 12463659 3 2011 201501 0
124636592 12463659 4 2012 0