The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
7915092 8010788 F 7915092-2 19960116 20111110 20111115 EXP US-MERCK-1106USA03370 MERCK HUMAN HEALTH DIVISION 56 YR F Y 66 KG 20111115 MD UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
7915092 1018050535 SS ALENDRONATE SODIUM 1 ORAL
7915092 1018050528 SS FOSAMAX 1 ORAL 020560
7915092 1018050531 SS FOSAMAX 1 ORAL 020560
7915092 1018050536 SS FOSAMAX PLUS D 1 ORAL
7915092 1018050537 SS FOSAMAX PLUS D 1 ORAL
7915092 1018050526 PS FOSAMAX 1 ORAL 020560
7915092 1018050529 SS FOSAMAX 1 ORAL 020560
7915092 1018050530 SS FOSAMAX 1 ORAL 020560
7915092 1018050532 C VITAMINS (UNSPECIFIED) 2 ORAL
7915092 1018050534 SS ALENDRONATE SODIUM 1 ORAL
7915092 1018050527 SS FOSAMAX 1 ORAL 020560
7915092 1018050533 C CALCIUM (UNSPECIFIED) 2 ORAL 1200-2000 MG DAILY

Indications of drugs used

Event ID DRUG SEQ INDI PT
7915092 1018050535 OSTEOPENIA
7915092 1018050536 OSTEOPOROSIS
7915092 1018050537 OSTEOPENIA
7915092 1018050526 OSTEOPOROSIS
7915092 1018050529 OSTEOPENIA
7915092 1018050534 OSTEOPOROSIS

Outcome of event

Event ID OUTC COD
7915092 HO
7915092 DS
7915092 OT

Reactions reported

Event ID PT
7915092 CALCIUM DEFICIENCY
7915092 CARPAL TUNNEL SYNDROME
7915092 SACROILIITIS
7915092 LOW TURNOVER OSTEOPATHY
7915092 SQUAMOUS CELL CARCINOMA OF SKIN
7915092 LUMBAR SPINAL STENOSIS
7915092 HYPERLIPIDAEMIA
7915092 FOOT FRACTURE
7915092 WOUND
7915092 SPINAL OSTEOARTHRITIS
7915092 MUSCLE STRAIN
7915092 FALL
7915092 BURSITIS
7915092 INSOMNIA
7915092 GASTROOESOPHAGEAL REFLUX DISEASE
7915092 DRY MOUTH
7915092 INTERVERTEBRAL DISC PROTRUSION
7915092 RESPIRATORY TRACT INFECTION
7915092 ARTHRALGIA
7915092 CONTUSION
7915092 HYPOCALCAEMIA
7915092 SINUSITIS
7915092 DRUG HYPERSENSITIVITY
7915092 NAIL AVULSION
7915092 CONSTIPATION
7915092 BLOOD PRESSURE INCREASED
7915092 ANOGENITAL WARTS
7915092 INTERVERTEBRAL DISC DISORDER
7915092 JOINT INJURY
7915092 VITAMIN D DEFICIENCY
7915092 MUSCULAR WEAKNESS
7915092 STRESS FRACTURE
7915092 OSTEOPOROSIS
7915092 INTERVERTEBRAL DISC DEGENERATION
7915092 HIP FRACTURE
7915092 CELLULITIS
7915092 BLOOD TRIGLYCERIDES INCREASED
7915092 SPINAL COLUMN STENOSIS
7915092 PAIN IN EXTREMITY
7915092 FEMUR FRACTURE
7915092 ABSCESS LIMB
7915092 BACK PAIN
7915092 RHINITIS ALLERGIC

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
7915092 1018050535 20090217 20100910 20 MON
7915092 1018050528 20021101 20070601 56 MON
7915092 1018050531 20021101 20070601 56 MON
7915092 1018050536 20070601 20090201 21 MON
7915092 1018050537 20070601 20090201 21 MON
7915092 1018050526 19951207 19980501 30 MON
7915092 1018050529 19951207 19980501 30 MON
7915092 1018050530 19980601 20021001 53 MON
7915092 1018050532 19700101
7915092 1018050534 20090217 20100910 20 MON
7915092 1018050527 19980601 20021001 53 MON
7915092 1018050533 19800101