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
127013351 12701335 1 I 2016 20160802 20160831 20160831 PER US-009507513-1608USA001900 MERCK 0.00 F Y 0.00000 20160831 PH 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
127013351 12701335 1 PS INTRON A INTERFERON ALFA-2B 1 Subcutaneous 17 MIU, 3 TIMES A WEEK (TIW) U M002230 103132 POWDER FOR INJECTION TIW
127013351 12701335 2 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
127013351 12701335 3 C ZOLOFT SERTRALINE HYDROCHLORIDE 1 0
127013351 12701335 4 C ZOFRAN ONDANSETRON HYDROCHLORIDE 1 0
127013351 12701335 5 C ESTRADIOL. ESTRADIOL 1 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127013351 12701335 1 Skin cancer

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127013351 12701335 Decreased appetite
127013351 12701335 Diarrhoea
127013351 12701335 Dysgeusia
127013351 12701335 Dyspnoea
127013351 12701335 Fatigue
127013351 12701335 Headache
127013351 12701335 Influenza like illness
127013351 12701335 Nausea
127013351 12701335 Palpitations
127013351 12701335 Weight decreased

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
127013351 12701335 1 201605 0