The Safety Rates Drug Report

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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
96529332 9652933 2 F 20160923 20131029 20160927 PER US-PFIZER INC-2013304495 PFIZER 60.00 YR F Y 0.00000 20160927 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
96529332 9652933 1 PS CLEOCIN CLINDAMYCIN PHOSPHATE 1 UNK U 50441
96529332 9652933 2 SS CLINDAMYCIN HCL CLINDAMYCIN HYDROCHLORIDE 1 UNK U 50162 CAPSULE, HARD
96529332 9652933 3 SS BUTORPHANOL TARTRATE. BUTORPHANOL TARTRATE 1 UNK U 74626
96529332 9652933 4 SS CODEINE CODEINE 1 UNK U 0
96529332 9652933 5 SS STADOL BUTORPHANOL TARTRATE 1 UNK U 0
96529332 9652933 6 SS FLEXERIL CYCLOBENZAPRINE HYDROCHLORIDE 1 UNK U 0
96529332 9652933 7 SS VALTREX VALACYCLOVIR HYDROCHLORIDE 1 UNK U 0
96529332 9652933 8 SS VIOXX ROFECOXIB 1 UNK U 0

Indications of drugs used

no results found

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
96529332 9652933 Drug hypersensitivity

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

no results found

Therapies reported

no results found