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
126245521 12624552 1 I 20150805 20150811 20160805 20160805 PER US-DRREDDYS-USA/USA/15/0050019 DR REDDYS 84.00 YR 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
126245521 12624552 1 PS Levofloxacin Tablets 750 mg LEVOFLOXACIN 1 Oral Y U UNKNOWN 76710 750 MG TABLET QD
126245521 12624552 2 SS CIPROFLOXACIN. CIPROFLOXACIN 1 Oral UNKNOWN 75593 1 DF TABLET
126245521 12624552 3 C MECLIZINE MECLIZINE HYDROCHLORIDE 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126245521 12624552 1 Cellulitis
126245521 12624552 2 Cellulitis
126245521 12624552 3 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126245521 12624552 Anxiety
126245521 12624552 Dyspnoea
126245521 12624552 Expired product administered
126245521 12624552 Lip swelling
126245521 12624552 Musculoskeletal pain
126245521 12624552 Neck pain
126245521 12624552 Peripheral swelling
126245521 12624552 Tendon pain
126245521 12624552 Vomiting

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
126245521 12624552 1 20150806 20150809 0
126245521 12624552 2 20150805 20150805 0