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
127710502 12771050 2 F 20160402 20160923 20160922 20160929 EXP US-DRREDDYS-USA/USA/16/0083346 DR REDDYS 23.00 YR F Y 77.11000 KG 20160929 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
127710502 12771050 1 PS Levofloxacin Tablets LEVOFLOXACIN 1 Oral Y U UNKNOWN 76710 750 MG TABLET QD
127710502 12771050 2 SS AMOXICILLIN. AMOXICILLIN 1 Unknown U U UNKNOWN 50754 TABLET
127710502 12771050 3 I ALBUTEROL. ALBUTEROL 1 Unknown INHALER UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127710502 12771050 1 Bronchitis
127710502 12771050 2 Product used for unknown indication
127710502 12771050 3 Bronchitis

Outcome of event

Event ID CASEID OUTC COD
127710502 12771050 OT
127710502 12771050 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127710502 12771050 Bronchitis
127710502 12771050 Chest pain
127710502 12771050 Drug interaction
127710502 12771050 Fatigue
127710502 12771050 Mitral valve incompetence
127710502 12771050 Muscle disorder
127710502 12771050 Myocarditis
127710502 12771050 Pericardial effusion
127710502 12771050 Pericarditis
127710502 12771050 Rhabdomyolysis
127710502 12771050 Sensory loss
127710502 12771050 Shock
127710502 12771050 Tachycardia
127710502 12771050 Tricuspid valve incompetence

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
127710502 12771050 1 20160401 0