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
127655311 12765531 1 I 201605 20160916 20160921 20160921 PER US-JNJFOC-20160918706 JANSSEN 85.74 YR E M Y 68.04000 KG 20160921 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
127655311 12765531 1 PS LEVAQUIN LEVOFLOXACIN 1 Unknown D N 20634 UNSPECIFIED
127655311 12765531 2 SS CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 Oral STRENGTH (36000 UNIT), 72000 UNIT, WITH EACH MEAL. 0 216000 IU CAPSULE
127655311 12765531 3 SS CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 Oral STRENGTH (24000 UNIT), 24000 UNIT, AS NEEDED WITH SNACKS. 0 72000 IU CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127655311 12765531 1 Atypical pneumonia
127655311 12765531 2 Pancreatic carcinoma
127655311 12765531 3 Pancreatic carcinoma

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127655311 12765531 Abdominal distension
127655311 12765531 Abdominal pain
127655311 12765531 Diarrhoea
127655311 12765531 Nausea
127655311 12765531 Vomiting
127655311 12765531 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
127655311 12765531 1 2016 0
127655311 12765531 2 2014 0
127655311 12765531 3 2014 0