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
125670781 12567078 1 I 20160620 20160718 20160718 PER US-PFIZER INC-2016310844 PFIZER 0.00 A M Y 0.00000 20160718 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
125670781 12567078 1 SS ACETYLSALICYLIC ACID ASPIRIN 1 UNK U 0
125670781 12567078 2 SS AMOXICILLIN. AMOXICILLIN 1 UNK U 0
125670781 12567078 3 PS BUTORPHANOL TARTRATE. BUTORPHANOL TARTRATE 1 UNK U 74626
125670781 12567078 4 SS CIPROFLOXACIN. CIPROFLOXACIN 1 UNK U 77245
125670781 12567078 5 SS CLARITHROMYCIN. CLARITHROMYCIN 1 UNK U 0
125670781 12567078 6 SS CLINDAMYCIN PHOSPHATE. CLINDAMYCIN PHOSPHATE 1 UNK U 50441
125670781 12567078 7 SS CODEINE CODEINE 1 UNK U 0
125670781 12567078 8 SS LEVOFLOXACIN. LEVOFLOXACIN 1 UNK U 78577
125670781 12567078 9 SS NITROFURANTOIN. NITROFURANTOIN 1 UNK U 0
125670781 12567078 10 SS TETRACYCLINE HCL TETRACYCLINE HYDROCHLORIDE 1 UNK U 60347
125670781 12567078 11 SS AMITRIPTYLINE AMITRIPTYLINE 1 UNK U 0
125670781 12567078 12 SS BUDESONIDE. BUDESONIDE 1 UNK U 0
125670781 12567078 13 SS IODINE. IODINE 1 Topical UNK U 0
125670781 12567078 14 SS HYDROCODONE HYDROCODONE 1 UNK U 0
125670781 12567078 15 SS CLAVULANATE POTASSIUM CLAVULANATE POTASSIUM 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
125670781 12567078 Drug hypersensitivity

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

no results found

Therapies reported

no results found