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
124088583 12408858 3 F 20160412 20160805 20160526 20160810 PER US-PFIZER INC-2016249908 PFIZER 30.00 YR F Y 127.10000 KG 20160810 MD 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
124088583 12408858 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 50 MG, 1X/DAY Y 21992 50 MG PROLONGED-RELEASE TABLET QD
124088583 12408858 2 C DEPLIN LEVOMEFOLATE CALCIUM 1 UNK 0
124088583 12408858 3 C ALLEGRA FEXOFENADINE HYDROCHLORIDE 1 UNK, DAILY 0
124088583 12408858 4 C PRILOSEC OMEPRAZOLE MAGNESIUM 1 UNK, DAILY 0
124088583 12408858 5 C LEXAPRO ESCITALOPRAM OXALATE 1 UNK 0
124088583 12408858 6 C PROPRANOLOL PROPRANOLOLPROPRANOLOL HYDROCHLORIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124088583 12408858 1 Major depression
124088583 12408858 2 Major depression
124088583 12408858 5 Major depression

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
124088583 12408858 Abdominal pain upper
124088583 12408858 Diarrhoea
124088583 12408858 Dyspepsia
124088583 12408858 Gastrooesophageal reflux disease
124088583 12408858 Headache
124088583 12408858 Hyperhidrosis
124088583 12408858 Nausea
124088583 12408858 Nightmare
124088583 12408858 Tremor

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
124088583 12408858 1 20160412 20160505 0
124088583 12408858 2 20160412 0
124088583 12408858 5 20160512 0
124088583 12408858 6 20160412 0