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
126245111 12624511 1 I 20160518 20160805 20160805 PER US-DRREDDYS-DRL/USA/16/0080183 DR REDDYS 0.00 F Y 0.00000 20160805 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
126245111 12624511 1 PS CIPROFLOXACIN. CIPROFLOXACIN 1 Unknown UNKNOWN 75593

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126245111 12624511 1 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126245111 12624511 Arthralgia
126245111 12624511 Burning sensation
126245111 12624511 Depressed mood
126245111 12624511 Dyspnoea
126245111 12624511 Fatigue
126245111 12624511 Gait disturbance
126245111 12624511 Hypersomnia
126245111 12624511 Pain in extremity

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
126245111 12624511 1 201508 0