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
99087194 9908719 4 F 20160914 20140219 20160920 PER US-PFIZER INC-2014046508 PFIZER 66.00 YR F Y 58.97000 KG 20160920 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
99087194 9908719 1 PS PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 100 MG, UNK D 21992 100 MG PROLONGED-RELEASE TABLET QD
99087194 9908719 2 C ALEVE NAPROXEN SODIUM 1 1000 MG, 1X/DAY 0 1000 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
99087194 9908719 1 Depression
99087194 9908719 2 Rheumatoid arthritis

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
99087194 9908719 Asthenia
99087194 9908719 Dizziness
99087194 9908719 Drug dose omission
99087194 9908719 Drug withdrawal syndrome
99087194 9908719 Feeling abnormal
99087194 9908719 Impaired driving ability
99087194 9908719 Impaired work ability
99087194 9908719 Malaise
99087194 9908719 Nervousness
99087194 9908719 Rebound effect

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

no results found

Therapies reported

no results found