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
122897132 12289713 2 F 20160303 20160901 20160421 20160915 EXP IT-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-115101 RANBAXY 52.16 YR M Y 0.00000 20160915 OT IT IT

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
122897132 12289713 1 PS AMOXICILLIN. AMOXICILLIN 1 Oral 1 G TOTAL Y U 0 1 G
122897132 12289713 2 C RATACAND PLUS 16/12,5 MG 2 Oral 1 DF U U 0 1 DF
122897132 12289713 3 C PANCREALIPASE PANCRELIPASE 1 U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122897132 12289713 1 Product used for unknown indication
122897132 12289713 2 Product used for unknown indication
122897132 12289713 3 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122897132 12289713 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122897132 12289713 Erythema
122897132 12289713 Pruritus generalised
122897132 12289713 Swollen tongue
122897132 12289713 Tongue coated

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
122897132 12289713 1 20160303 20160303 0