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
71566762 7156676 2 F 20160629 20160701 20091023 20160706 EXP US-PFIZER INC-2009284442 PFIZER 51.00 YR F Y 59.00000 KG 20160706 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
71566762 7156676 1 PS ZOLOFT SERTRALINE HYDROCHLORIDE 1 25 MG, UNK Y Y C081291 19839 25 MG
71566762 7156676 2 SS ZOLOFT SERTRALINE HYDROCHLORIDE 1 50 MG, UNK Y Y 19839 50 MG
71566762 7156676 3 SS ZOLOFT SERTRALINE HYDROCHLORIDE 1 Oral 25 MG, 1X/DAY Y Y 19839 25 MG QD
71566762 7156676 4 C ADVIL IBUPROFEN 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
71566762 7156676 1 Anxiety
71566762 7156676 2 Depression
71566762 7156676 3 Nervousness
71566762 7156676 4 Dysmenorrhoea

Outcome of event

Event ID CASEID OUTC COD
71566762 7156676 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
71566762 7156676 Anger Anger
71566762 7156676 Drug dose omission
71566762 7156676 Drug ineffective
71566762 7156676 Drug withdrawal syndrome
71566762 7156676 Fatigue Fatigue
71566762 7156676 Middle insomnia Middle insomnia
71566762 7156676 Nightmare Nightmare
71566762 7156676 Panic attack Panic attack
71566762 7156676 Personality change Personality change
71566762 7156676 Product taste abnormal
71566762 7156676 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

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
71566762 7156676 1 2004 0