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
126739402 12673940 2 F 201603 20160822 20160822 20160826 EXP US-ABBVIE-16P-163-1704426-00 ABBVIE 46.32 YR F Y 0.00000 20160826 OT COUNTRY NOT SPECIFIED 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
126739402 12673940 1 PS CREON PANCRELIPASE AMYLASEPANCRELIPASE LIPASEPANCRELIPASE PROTEASE 1 Oral 5-6 CAPSULE WITH EACH MEAL U UNKNOWN 20725 CAPSULE
126739402 12673940 2 C NEXIUM ESOMEPRAZOLE MAGNESIUM 1 Unknown 0
126739402 12673940 3 C HYOSCYAMINE. HYOSCYAMINE 1 Unknown 0
126739402 12673940 4 C NUVIGIL ARMODAFINIL 1 Unknown 0
126739402 12673940 5 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126739402 12673940 1 Pancreatitis chronic
126739402 12673940 2 Gastrooesophageal reflux disease
126739402 12673940 3 Muscle spasms
126739402 12673940 4 Somnolence
126739402 12673940 5 Pain

Outcome of event

Event ID CASEID OUTC COD
126739402 12673940 HO
126739402 12673940 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126739402 12673940 Coma
126739402 12673940 Memory impairment

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
126739402 12673940 1 201505 201605 0