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
125218761 12521876 1 I 20160509 20160620 20160701 20160701 EXP US-BAYER-2016-125890 BAYER 43.00 YR A F Y 77.98000 KG 20160701 CN 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
125218761 12521876 1 PS CIPRO CIPROFLOXACIN HYDROCHLORIDE 1 UNK 21473 MODIFIED-RELEASE FILM-COATED TABLET
125218761 12521876 2 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 0 10 MG BID
125218761 12521876 3 C REBIF INTERFERON BETA-1A 1 UNK 0
125218761 12521876 4 C VITAMIN B12 CYANOCOBALAMIN 1 0
125218761 12521876 5 C MAGNESIUM MAGNESIUM 1 200 MG 0
125218761 12521876 6 C SERTRALINE HYDROCHLORIDE. SERTRALINE HYDROCHLORIDE 1 100 MG 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125218761 12521876 1 Cystitis
125218761 12521876 2 Gait disturbance

Outcome of event

Event ID CASEID OUTC COD
125218761 12521876 DS
125218761 12521876 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125218761 12521876 Abdominal pain upper
125218761 12521876 Balance disorder
125218761 12521876 Condition aggravated
125218761 12521876 Limb discomfort
125218761 12521876 Muscle fatigue
125218761 12521876 Nausea
125218761 12521876 Tongue pruritus

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
125218761 12521876 1 20160509 0
125218761 12521876 2 20160420 0
125218761 12521876 3 201602 0