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
7023066 5669451 F 7023066-1 20030101 20100916 20100930 EXP PHEH2004US10740 NOVARTIS PHARMACEUTICAL CORPORATION YR Y 20100930 OT 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
7023066 1014812499 PS ZOMETA 1 INTRAVENOUS MONTHLY 021223
7023066 1014812500 C ARIMIDEX 1
7023066 1014812501 C GLUCOVANCE 1
7023066 1014812502 C PREDNISONE 2
7023066 1014812503 C MONOPRIL 1
7023066 1014812504 C DOXEPIN HCL 1
7023066 1014812505 C WELLBUTRIN 1
7023066 1014812506 C OXYCONTIN 1 80 MG, QD
7023066 1014812507 C NEURONTIN 1
7023066 1014812508 C HYDROCHLOROTHIAZIDE 2
7023066 1014812509 C POTASSIUM CHLORIDE 2
7023066 1014812510 C XANAX 1
7023066 1014812511 C TEMAZEPAM 1
7023066 1014812512 C PHENERGAN ^AVENTIS PHARMA^ 2
7023066 1014812513 C IBUPROFEN 2
7023066 1014812514 C BLACK COHOSH 2
7023066 1014812515 C IRON 2
7023066 1014812516 C ZOLADEX 1
7023066 1014812517 C GLYBURIDE AND METFORMIN HCL 1
7023066 1014812518 C ALFAXALONE 2
7023066 1014812519 C PROMETHAZINE 2
7023066 1014812520 C ASPIRIN 1
7023066 1014812521 C MOTRIN 1
7023066 1014812522 C VICOPROFEN 1
7023066 1014812523 C REGLAN 1
7023066 1014812524 C OXYCODONE 2
7023066 1014812525 C ZYRTEC 1
7023066 1014812526 C SEPTRA 1
7023066 1014812527 C TOPROL-XL 1
7023066 1014812528 C AUGMENTIN '125' 1
7023066 1014812529 C VICODIN 1
7023066 1014812530 C VIOXX 1
7023066 1014812531 C PAXIL 1
7023066 1014812532 C XANAX 1
7023066 1014812533 C DIOVAN 1
7023066 1014812534 C LEXAPRO 1
7023066 1014812535 C METFORMIN 2
7023066 1014812536 C RIFAMPIN 1
7023066 1014812537 C ALLEGRA 1
7023066 1014812538 C LANTUS 1
7023066 1014812539 C ALPRAZOLAM 2
7023066 1014812540 C DOXEPIN HCL 1
7023066 1014812541 C BENADRYL ^PFIZER WARNER-LAMBERT^ 2
7023066 1014812542 C OXYCODONE HCL 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
7023066 1014812499 METASTASES TO BONE
7023066 1014812500 BREAST CANCER
7023066 1014812501 DIABETES MELLITUS
7023066 1014812503 HYPERTENSION
7023066 1014812504 DEPRESSION
7023066 1014812505 DEPRESSION
7023066 1014812506 BONE PAIN

Outcome of event

Event ID OUTC COD
7023066 HO
7023066 OT

Reactions reported

Event ID PT
7023066 ABDOMINAL PAIN
7023066 ACCOMMODATION DISORDER
7023066 ADENOMYOSIS
7023066 ALTERED VISUAL DEPTH PERCEPTION
7023066 ANAEMIA
7023066 ARTHRALGIA
7023066 ARTHROPATHY
7023066 BACK PAIN
7023066 BONE DEBRIDEMENT
7023066 CELLULITIS
7023066 COCCYDYNIA
7023066 CONSTIPATION
7023066 COUGH
7023066 CULDOPLASTY
7023066 DENTAL CARIES
7023066 DIABETES MELLITUS
7023066 DIPLOPIA
7023066 DYSPNOEA
7023066 ENDODONTIC PROCEDURE
7023066 EXCORIATION
7023066 EYE PAIN
7023066 FACIAL PAIN
7023066 FATIGUE
7023066 GINGIVAL DISORDER
7023066 GINGIVAL PAIN
7023066 HEPATIC STEATOSIS
7023066 HOT FLUSH
7023066 HYPOGLYCAEMIA
7023066 HYPOKALAEMIA
7023066 HYPOXIA
7023066 HYSTERECTOMY
7023066 INTERVERTEBRAL DISC DEGENERATION
7023066 INTERVERTEBRAL DISC PROTRUSION
7023066 IRON DEFICIENCY ANAEMIA
7023066 JAW DISORDER
7023066 JOINT SWELLING
7023066 LACRIMATION INCREASED
7023066 LUNG NEOPLASM
7023066 LYMPHOEDEMA
7023066 MIGRAINE
7023066 MOUTH ULCERATION
7023066 NASAL CONGESTION
7023066 NAUSEA
7023066 NEPHROLITHIASIS
7023066 NEURODERMATITIS
7023066 OEDEMA
7023066 OSTEONECROSIS OF JAW
7023066 PAIN
7023066 PAIN IN JAW
7023066 PARAESTHESIA
7023066 PELVIC FLOOR MUSCLE WEAKNESS
7023066 PYREXIA
7023066 RASH
7023066 RECTOCELE REPAIR
7023066 RENAL FAILURE
7023066 RETINOPATHY
7023066 SEPSIS
7023066 SKIN DISORDER
7023066 SPLINT APPLICATION
7023066 TONGUE INJURY
7023066 TOOTH DISORDER
7023066 TOOTH EXTRACTION
7023066 ULCER
7023066 URETERAL DISORDER
7023066 UTERINE HAEMORRHAGE
7023066 VENOUS ANGIOMA OF BRAIN
7023066 VERTIGO
7023066 VISION BLURRED
7023066 VISUAL IMPAIRMENT
7023066 VITREOUS FLOATERS
7023066 VOMITING
7023066 WEIGHT INCREASED
7023066 WITHDRAWAL SYNDROME
7023066 WOUND
7023066 WOUND INFECTION STAPHYLOCOCCAL

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
7023066 1014812499 20010101 20040601
7023066 1014812506 20010101