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
100123184 10012318 4 F 20160308 20140312 20160331 PER US-PFIZER INC-2014069035 PFIZER 0.00 F Y 0.00000 20160331 MD 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
100123184 10012318 1 PS CLEOCIN CLINDAMYCIN PHOSPHATE 1 Oral UNK, 1-2 DOSES 50162 CAPSULE, HARD
100123184 10012318 2 SS MORPHINE SULFATE. MORPHINE SULFATE 1 Oral UNK, 1-2 DOSES 19999
100123184 10012318 3 SS CODEINE CODEINE 1 Oral UNK, 1-2 DOSES 0
100123184 10012318 4 SS VICODIN ACETAMINOPHENHYDROCODONE BITARTRATE 1 Oral UNK, 1-2 DOSES 0
100123184 10012318 5 SS HYDROCODONE HYDROCODONE 1 Oral UNK, 1-2 DOSES 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100123184 10012318 1 Infection
100123184 10012318 2 Pain
100123184 10012318 3 Pain
100123184 10012318 4 Pain
100123184 10012318 5 Pain

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
100123184 10012318 Drug hypersensitivity
100123184 10012318 Pharyngeal oedema
100123184 10012318 Urticaria

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

no results found

Therapies reported

no results found