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
110318533 11031853 3 F 20160822 20150415 20160823 PER US-BAYER-2015-103804 BAYER 56.00 YR A F Y 101.59000 KG 20160823 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
110318533 11031853 1 PS AVELOX MOXIFLOXACIN HYDROCHLORIDE 1 UNK 21085 FILM-COATED TABLET
110318533 11031853 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral 500 MG, UNK 0 500 MG
110318533 11031853 3 C BUPRENORPHINE. BUPRENORPHINE 1 0
110318533 11031853 4 C GABAPENTIN. GABAPENTIN 1 0
110318533 11031853 5 C TIZANIDINE. TIZANIDINE 1 0
110318533 11031853 6 C DULOXETINE. DULOXETINE 1 0
110318533 11031853 7 C LEVOTHYROXINE. LEVOTHYROXINE 1 0
110318533 11031853 8 C SYMBICORT BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE 1 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
110318533 11031853 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
110318533 11031853 Anxiety
110318533 11031853 Bone pain
110318533 11031853 Burning sensation
110318533 11031853 Emotional distress
110318533 11031853 Fear
110318533 11031853 Hypoaesthesia
110318533 11031853 Injury
110318533 11031853 Muscle spasms
110318533 11031853 Muscle twitching
110318533 11031853 Neuropathy peripheral
110318533 11031853 Pain
110318533 11031853 Quality of life decreased

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
110318533 11031853 1 201308 0
110318533 11031853 2 20140126 20150105 0