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
126948361 12694836 1 I 20160822 20160829 20160829 EXP CA-MYLANLABS-2016M1035941 MYLAN 0.00 Y 0.00000 20160829 CN CA CA

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
126948361 12694836 1 PS CYANOCOBALAMIN. CYANOCOBALAMIN 1 UNK U 40451 INJECTION
126948361 12694836 2 SS TWINRIX HEPATITIS A VIRUS STRAIN HM175 ANTIGEN (FORMALDEHYDE INACTIVATED)HEPATITIS B VIRUS SUBTYPE ADW2 HBSAG SURFACE PROTEIN ANTIGEN 1 U 0 SUSPENSION FOR INJECTION
126948361 12694836 3 SS MACROBID NITROFURANTOINNITROFURANTOIN MONOHYDRATE 1 U 0 CAPSULE

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126948361 12694836 1 Product used for unknown indication
126948361 12694836 2 Prophylaxis
126948361 12694836 3 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126948361 12694836 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126948361 12694836 Burning sensation
126948361 12694836 Hypoaesthesia
126948361 12694836 Multiple sclerosis
126948361 12694836 Myelitis transverse

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

no results found

Therapies reported

no results found