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
87716142 8771614 2 F 2003 20160720 20120905 20160725 EXP US-009507513-1104USA02224 MERCK 0.00 F Y 75.30000 KG 20160725 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
87716142 8771614 1 PS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
87716142 8771614 2 SS FOSAMAX ALENDRONATE SODIUM 1 Oral 70 MG, QW U 20560 70 MG TABLET /wk
87716142 8771614 3 SS ALENDRONATE SODIUM. ALENDRONATE SODIUM 1 Oral 70 MG, QW 20560 70 MG TABLET /wk
87716142 8771614 4 C VITAMINS (UNSPECIFIED) VITAMINS 1 Oral 1 UNK, UNK U 0 1 DF
87716142 8771614 5 C CALCIUM (UNSPECIFIED) (+) VITAMIN D (UNSPECIFIED) CALCIUM CARBONATEVITAMIN D 1 Unknown 1200 MG, UNKNOWN U 0 1200 MG
87716142 8771614 6 C OMEGA-3 MARINE TRIGLYCERIDES FISH OIL 1 Unknown 3000 MG, UNKNOWN U 0 3000 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
87716142 8771614 1 Osteoporosis
87716142 8771614 2 Osteoporosis
87716142 8771614 3 Osteoporosis
87716142 8771614 4 Routine health maintenance
87716142 8771614 5 Routine health maintenance
87716142 8771614 6 Routine health maintenance

Outcome of event

Event ID CASEID OUTC COD
87716142 8771614 HO
87716142 8771614 DS
87716142 8771614 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
87716142 8771614 Acute respiratory failure
87716142 8771614 Anaemia
87716142 8771614 Angina pectoris
87716142 8771614 Anxiety
87716142 8771614 Arteriosclerosis coronary artery
87716142 8771614 Arthralgia
87716142 8771614 Arthritis
87716142 8771614 Arthropathy
87716142 8771614 Blood cholesterol increased
87716142 8771614 Body mass index increased
87716142 8771614 Cellulitis
87716142 8771614 Chest pain
87716142 8771614 Chronic obstructive pulmonary disease
87716142 8771614 Constipation
87716142 8771614 Depression
87716142 8771614 Device failure
87716142 8771614 Drug hypersensitivity
87716142 8771614 Fall
87716142 8771614 Femur fracture
87716142 8771614 Foot fracture
87716142 8771614 Fracture delayed union
87716142 8771614 Fracture nonunion
87716142 8771614 Gastrooesophageal reflux disease
87716142 8771614 Haematoma
87716142 8771614 Headache
87716142 8771614 Hypercholesterolaemia
87716142 8771614 Hypertension
87716142 8771614 Impaired healing
87716142 8771614 Insomnia
87716142 8771614 Intervertebral disc degeneration
87716142 8771614 Joint swelling
87716142 8771614 Musculoskeletal pain
87716142 8771614 Osteoarthritis
87716142 8771614 Pain in extremity
87716142 8771614 Pneumonia
87716142 8771614 Rib fracture
87716142 8771614 Seroma
87716142 8771614 Spinal column stenosis
87716142 8771614 Spinal compression fracture
87716142 8771614 Suicidal ideation
87716142 8771614 Tendonitis
87716142 8771614 Tenosynovitis
87716142 8771614 Tooth disorder

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
87716142 8771614 1 20030115 200410 0
87716142 8771614 3 200410 201010 0
87716142 8771614 4 1992 0
87716142 8771614 5 1992 0