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
92936422 9293642 2 F 20100518 20160728 20130516 20160805 EXP US-009507513-1305USA007042 MERCK 0.00 F Y 0.00000 20160805 MD 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
92936422 9293642 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 35 MG, UNK 20560 35 MG TABLET
92936422 9293642 2 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 35 MG, UNK 20560 35 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
92936422 9293642 1 Product used for unknown indication
92936422 9293642 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
92936422 9293642 OT
92936422 9293642 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
92936422 9293642 Dehydration
92936422 9293642 Ecchymosis
92936422 9293642 Haemorrhagic anaemia
92936422 9293642 Hip fracture
92936422 9293642 Hyperlipidaemia
92936422 9293642 Hypertension
92936422 9293642 Hysterectomy
92936422 9293642 Malignant melanoma
92936422 9293642 Osteoarthritis
92936422 9293642 Rhabdomyolysis
92936422 9293642 Troponin increased
92936422 9293642 Ventricular extrasystoles

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
92936422 9293642 1 20040118 20070716 0
92936422 9293642 2 20080330 20100404 0