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
127201221 12720122 1 I 2005 20160831 20160907 20160907 PER US-PFIZER INC-2016413485 PFIZER 37.00 YR M Y 0.00000 20160907 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
127201221 12720122 1 PS ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 25 MG, UNK U 19839 25 MG FILM-COATED TABLET
127201221 12720122 2 SS ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 50 MG, UNK U 19839 50 MG FILM-COATED TABLET
127201221 12720122 3 SS ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 100 MG, UNK U 19839 100 MG FILM-COATED TABLET
127201221 12720122 4 SS ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 50MG TABLET ONCE DAILY U 19839 50 MG FILM-COATED TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127201221 12720122 1 Depressive symptom

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127201221 12720122 Anxiety
127201221 12720122 Dizziness
127201221 12720122 Drug ineffective
127201221 12720122 Headache
127201221 12720122 Malaise
127201221 12720122 Nausea

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

no results found

Therapies reported

no results found