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Forteo Side Effects Report #5649091-0
Consumer or non-health professional from UNITED STATES reported FORTEO problem on Feb 20, 2008. Female patient was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: bone density decreased, cerebral haemorrhage, nasopharyngitis, . FORTEO dosage: unknown. Patient was hospitalized. Patient died on 11/16/2006.

Forteo Side Effects Report #5649143-5
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 25, 2008. Female patient, 74 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: bone density decreased, dizziness, facial bones fracture, fall, inner ear disorder, loss of consciousness, nausea, patella fracture, . FORTEO dosage: unknown. During the same period patient was treated with ACTONEL. Patient recovered.

Evista Side Effects Report #5653903-4
Consumer or non-health professional from UNITED STATES reported EVISTA problem on Feb 25, 2008. Female patient was treated with EVISTA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, neoplasm, . EVISTA dosage: 60 MG, UNK. Patient recovered.

Boniva Side Effects Report #5661553-9
BONIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 03, 2008. Female patient, 54 years of age, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, multiple myeloma, . BONIVA dosage: unknown. During the same period patient was treated with SYNTHROID, NITROFURANTOIN. Patient recovered.


Fosamax Side Effects Report #5662280-4
Consumer or non-health professional from AUSTRALIA reported FOSAMAX problem on Mar 06, 2008. Female patient, 65 years of age, weighting 167.6 lb, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, impaired healing, myocardial infarction, pelvic fracture, tendon rupture, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5669366-9
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 04, 2008. Female patient, 58 years of age, weighting 105.8 lb, was diagnosed with osteoporosis prophylaxis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, ear pain, incision site infection, insomnia, malaise, nausea, osteomyelitis, osteonecrosis, osteopetrosis, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Coumadin Side Effects Report #5675071-5
Physician from UNITED STATES reported COUMADIN problem on Mar 18, 2008. Male patient, 60 years of age, was diagnosed with phlebitis, pulmonary embolism, vena cava filter insertion and was treated with COUMADIN. After drug was administered, patient experienced the following problems/side effects: bone density decreased, dermatitis, vena cava thrombosis, venous pressure increased, . COUMADIN dosage: unknown. During the same period patient was treated with CALCIUM, VITAMIN D. Patient recovered.

Forteo Side Effects Report #5677538-2
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 16, 2008. Female patient, 74 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: bone density decreased, dizziness, facial bones fracture, fall, inner ear disorder, loss of consciousness, nausea, patella fracture, . FORTEO dosage: unknown. During the same period patient was treated with ACTONEL. Patient recovered.

Flovent Side Effects Report #5680645-1
Consumer or non-health professional from UNITED STATES reported FLOVENT problem on Jan 24, 2008. Female patient, 62 years of age, was diagnosed with asthma and was treated with FLOVENT. After drug was administered, patient experienced the following problems/side effects: bone density decreased, nervousness, . FLOVENT dosage: unknown. During the same period patient was treated with PREDNISONE. Patient recovered.


Zometa Side Effects Report #5683054-4
ZOMETA problem was reported by a Physician from JAPAN on Mar 21, 2008. Male patient, 63 years of age, weighting 156.5 lb, was diagnosed with multiple myeloma, hypertension and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, bone disorder, dental treatment, disease progression, gingival disorder, osteonecrosis, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with MELPHALAN, DIOVAN, DEPAS, MUCOSOLVAN, WARFARIN, FAMOTIDINE, ALKERAN. Patient recovered.

Remicade Side Effects Report #5688255-7
Consumer or non-health professional from UNITED STATES reported REMICADE problem on Mar 18, 2008. Female patient, weighting 175.0 lb, was diagnosed with rheumatoid arthritis, panic attack, insomnia, depression and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: bone density decreased, breast mass, hospitalisation, nasopharyngitis, rash, . REMICADE dosage: unknown. During the same period patient was treated with METHOTREXATE, VALIUM, RESTORIL, ZOLOFT, CYMBALTA, FENTANYL. Patient was hospitalized. Patient recovered.

Evista Side Effects Report #5616441-0
EVISTA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 28, 2008. Female patient, 83 years of age, was diagnosed with osteoporosis and was treated with EVISTA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, femur fracture, foot fracture, . EVISTA dosage: unknown. During the same period patient was treated with CALTRATE. Patient recovered.

Fosamax Side Effects Report #5638825-7
Physician from UNITED STATES reported FOSAMAX problem on Feb 15, 2008. Female patient, 58 years of age, weighting 105.8 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, ear pain, insomnia, nausea, osteomyelitis, osteonecrosis, osteopetrosis, pain in jaw, sinusitis, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Zoledronic Side Effects Report #5642868-7
ZOLEDRONIC ACID problem was reported by a Physician from UNITED STATES on Feb 20, 2008. Female patient, 67 years of age, weighting 127.4 lb, was diagnosed with metastases to bone, breast cancer, prophylaxis, cardiomyopathy, oedema peripheral and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: bone density decreased, fall, femoral neck fracture, hip arthroplasty, osteoporosis, . ZOLEDRONIC ACID dosage: unknown. During the same period patient was treated with FEMARA, ASPIRIN, COREG, FUROSEMIDE, VITAMIN D, CALCIUM, ASCORBIC ACID, VITAMIN CAP. Patient was hospitalized. Patient recovered.


Fosamax Side Effects Report #5646070-4
Consumer or non-health professional from AUSTRALIA reported FOSAMAX problem on Feb 21, 2008. Female patient, 59 years of age, weighting 154.3 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, osteonecrosis, thyroid cancer, vocal cord neoplasm, . FOSAMAX dosage: unknown. Patient recovered.

Evista Side Effects Report #5578656-X
EVISTA problem was reported by a Physician from UNITED STATES on Dec 21, 2007. Female patient was diagnosed with osteoporosis and was treated with EVISTA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, meniere's disease, osteopenia, retinal haemorrhage, retinal vein thrombosis, . EVISTA dosage: 60 MG, UNK. During the same period patient was treated with ASPIRIN, CALCIUM, VITAMIN D, HYDROCHLOROTHIAZIDE. Patient recovered.

Thyroid Side Effects Report #5587634-6
Physician from UNITED STATES reported THYROID problem on Jan 02, 2008. Female patient, 57 years of age, was diagnosed with hypothyroidism and was treated with THYROID. After drug was administered, patient experienced the following problems/side effects: bone density decreased, resorption bone increased, . THYROID dosage: 90 MG QOD PO. Patient recovered.

Evista Side Effects Report #5597663-4
EVISTA problem was reported by a Physician from UNITED STATES on Jan 09, 2008. Female patient, 65 years of age, was treated with EVISTA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, breast cancer in situ, . EVISTA dosage: 60 MG, DAILY (1/D). During the same period patient was treated with VITAMIN D, CALCIUM GLUCONATE. Patient recovered.

Zometa Side Effects Report #5598109-2
Consumer or non-health professional from FRANCE reported ZOMETA problem on Jan 14, 2008. Male patient, 87 years of age, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, gingival ulceration, osteonecrosis, pain in jaw, . ZOMETA dosage: 4 MG EVERY 4 WEEKS. During the same period patient was treated with CLASTOBAN, ANANDRON, DECAPEPTYL. Patient was hospitalized. Patient recovered.


Coumadin Side Effects Report #5599777-1
COUMADIN problem was reported by a Physician from UNITED STATES on Jan 17, 2008. Male patient, 60 years of age, was diagnosed with phlebitis, pulmonary embolism, vena cava filter insertion and was treated with COUMADIN. After drug was administered, patient experienced the following problems/side effects: bone density decreased, dermatitis, vena cava thrombosis, venous pressure increased, . COUMADIN dosage: unknown. During the same period patient was treated with CALCIUM GLUCONATE, VITAMIN D. Patient recovered.

Evista Side Effects Report #5604371-X
Consumer or non-health professional from UNITED STATES reported EVISTA problem on Jan 14, 2008. Female patient was diagnosed with osteoporosis and was treated with EVISTA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, cataract, diabetes mellitus, glycosylated haemoglobin increased, osteopenia, osteoporosis, stress, . EVISTA dosage: 60 MG, UNK. During the same period patient was treated with FORTEO, CALTRATE. Patient recovered.

Evista Side Effects Report #5609285-7
EVISTA problem was reported by a Physician from UNITED STATES on Jan 25, 2008. Female patient, 65 years of age, was treated with EVISTA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, breast cancer in situ, . EVISTA dosage: 60 MG, DAILY (1/D). During the same period patient was treated with VITAMIN D, CALCIUM GLUCONATE. Patient recovered.

Cerezyme Side Effects Report #5614614-4
Consumer or non-health professional from UNITED STATES reported CEREZYME problem on Jan 16, 2008. Male patient, 63 years of age, weighting 169.3 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: bone density decreased, tooth loss, . CEREZYME dosage: unknown. Patient recovered.

Byetta Side Effects Report #5648001-X
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 27, 2007. Female patient, 65 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, dysgeusia, . BYETTA dosage: unknown. Patient recovered.

Decadron Side Effects Report #5532664-3
Consumer or non-health professional from UNITED STATES reported DECADRON problem on Nov 28, 2007. Male patient, 44 years of age, was diagnosed with brain neoplasm and was treated with DECADRON. After drug was administered, patient experienced the following problems/side effects: bone density decreased, hallucination, lung infection, muscle twitching, muscular weakness, . DECADRON dosage: unknown. During the same period patient was treated with TEMODAR, BACTRIM, LOPRESSOR. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5551645-7
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 29, 2007. Male patient was diagnosed with lymphoma and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: bone density decreased, dyspnoea, lymphocytic leukaemia, lymphoma, malaise, pleural effusion, spinal fracture, wound, . FORTEO dosage: unknown. During the same period patient was treated with RITUXAN, PREDNISONE, ACTONEL. Patient recovered.

Humira Side Effects Report #5560730-5
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Nov 21, 2007. Female patient, weighting 110.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, . HUMIRA dosage: unknown. During the same period patient was treated with EPOGEN. Patient recovered.

Zoledronic Side Effects Report #5564294-1
ZOLEDRONIC ACID problem was reported by a Physician from UNITED STATES on Dec 07, 2007. Female patient, 67 years of age, weighting 200.6 lb, was diagnosed with breast cancer, osteoporosis and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: bone density decreased, fall, open reduction of fracture, radius fracture, ulna fracture, upper limb fracture, . ZOLEDRONIC ACID dosage: 4MG EVERY 6 MONTHS. During the same period patient was treated with CALCIUM, VITAMIN D, FEMARA. Patient was hospitalized. Patient recovered.

Viread Side Effects Report #5565751-4
Physician from FRANCE reported VIREAD problem on Dec 06, 2007. Female patient, weighting 132.3 lb, was diagnosed with hiv infection and was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: bone density decreased, fanconi syndrome acquired, foot fracture, hypophosphataemia, neuropathy peripheral, pancreatitis acute, unevaluable event, . VIREAD dosage: unknown. During the same period patient was treated with VIDEX, EPIVIR, REYATAZ. Patient was hospitalized. Patient recovered.

Zoledronic Side Effects Report #5573069-9
ZOLEDRONIC ACID problem was reported by a Physician from UNITED STATES on Dec 18, 2007. Female patient, 67 years of age, weighting 200.6 lb, was diagnosed with breast cancer, osteoporosis and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: bone density decreased, concomitant disease progression, fall, open reduction of fracture, radius fracture, ulna fracture, upper limb fracture, . ZOLEDRONIC ACID dosage: 4MG EVERY 6 MONTHS. During the same period patient was treated with CALCIUM, VITAMIN D, FEMARA. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5578487-0
Consumer or non-health professional from AUSTRALIA reported FOSAMAX problem on Dec 28, 2007. Female patient, 75 years of age, weighting 180.8 lb, was diagnosed with osteoporosis, hypertension, duodenal ulcer and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, fall, rib fracture, spinal fracture, . FOSAMAX dosage: unknown. During the same period patient was treated with CALCIUM CARBONATE. Patient was hospitalized. Patient recovered.

Zoledronic Side Effects Report #5503673-5
ZOLEDRONIC ACID problem was reported by a Physician from UNITED STATES on Oct 25, 2007. Female patient, 67 years of age, weighting 200.6 lb, was diagnosed with breast cancer, osteoporosis and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: bone density decreased, fall, open reduction of fracture, radius fracture, ulna fracture, upper limb fracture, . ZOLEDRONIC ACID dosage: 4MG EVERY 6 MONTHS. During the same period patient was treated with CALCIUM, VITAMIN D, FEMARA. Patient was hospitalized. Patient recovered.

Detrol Side Effects Report #5504382-9
Consumer or non-health professional from UNITED STATES reported DETROL LA problem on Oct 23, 2007. Male patient, weighting 165.3 lb, was diagnosed with hypertonic bladder, back injury and was treated with DETROL LA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, micturition urgency, . DETROL LA dosage: unknown. During the same period patient was treated with CORTISONE ACETATE, ATENOLOL, VASOTEC, AVAPRO, ZOCOR, TRAMADOL, TYLENOL. Patient recovered.

Zometa Side Effects Report #5504840-7
ZOMETA problem was reported by a Physician from JAPAN on Oct 25, 2007. Male patient, 63 years of age, weighting 156.5 lb, was diagnosed with multiple myeloma, hypertension and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, bone disorder, dental treatment, disease progression, gingival disorder, osteonecrosis, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with MELPHALAN, DIOVAN, DEPAS, MUCOSOLVAN, WARFARIN, FAMOTIDINE, ALKERAN. Patient recovered.

Evista Side Effects Report #5507506-2
Physician from UNITED STATES reported EVISTA problem on Oct 24, 2007. Female patient was treated with EVISTA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, breast cancer, . EVISTA dosage: 60 MG, UNK. Patient recovered.

Aromasin Side Effects Report #5514695-2
AROMASIN problem was reported by a Consumer or non-health professional from JAPAN on Nov 05, 2007. Female patient, 56 years of age, was treated with AROMASIN. After drug was administered, patient experienced the following problems/side effects: bone density decreased, joint stiffness, normal tension glaucoma, . AROMASIN dosage: unknown. Patient recovered.

Zoledronic Side Effects Report #5518014-7
Physician from UNITED STATES reported ZOLEDRONIC ACID problem on Nov 06, 2007. Female patient, 67 years of age, weighting 200.6 lb, was diagnosed with breast cancer, osteoporosis and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: bone density decreased, fall, open reduction of fracture, radius fracture, ulna fracture, upper limb fracture, . ZOLEDRONIC ACID dosage: 4MG EVERY 6 MONTHS. During the same period patient was treated with CALCIUM, VITAMIN D, FEMARA. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5520081-1
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 15, 2007. Male patient, 57 years of age, weighting 286.6 lb, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: bone density decreased, dehydration, diarrhoea, influenza like illness, nausea, spinal fracture, staphylococcal bacteraemia, vomiting, white blood cell count decreased, . BETASERON dosage: unknown. During the same period patient was treated with PREDNISONE, IMURAN, ALLOPURINOL, CATAPRES, COZAAR, VERAPAMIL, METFORMIN. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5531924-X
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Nov 28, 2007. Female patient, 64 years of age, weighting 120.0 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, . FOSAMAX dosage: 70MG. Patient recovered.

Fosamax Side Effects Report #5573313-8
FOSAMAX problem was reported by a Consumer or non-health professional from UNITED STATES on June 29, 2007. Female patient, 54 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, myalgia, osteonecrosis, pericoronitis, . FOSAMAX dosage: 70 MG WKY PO. Patient recovered.

Fosamax Side Effects Report #5582544-2
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Mar 12, 2007. Female patient, 67 years of age, weighting 93.00 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, osteomyelitis, osteonecrosis, synovial cyst, synovitis, tenosynovitis, wrist fracture, . FOSAMAX dosage: 10 MG/DAILY/PO. During the same period patient was treated with EVISTA, LUMIGAN, NORVASC, PANCREASE, REMICADE, VOLTAREN. Patient recovered.

Fosamax Side Effects Report #5584388-4
FOSAMAX problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 18, 2006. Female patient, 71 years of age, was diagnosed with osteopenia, osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, osteomyelitis, osteonecrosis, . FOSAMAX dosage: 10 MG/DAILY/PO. Patient recovered.

Arimidex Side Effects Report #5472594-9
Consumer or non-health professional from UNITED STATES reported ARIMIDEX problem on July 19, 2006. Female patient, 58 years of age, weighting 130.1 lb, was diagnosed with breast cancer female and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, dyspnoea, oedema peripheral, oral pruritus, stomatitis, tongue eruption, . ARIMIDEX dosage: unknown. During the same period patient was treated with ACTONEL, ACYCLOVIR. Patient recovered.

Arimidex Side Effects Report #5473585-4
ARIMIDEX problem was reported by a Consumer or non-health professional from UNITED STATES on July 16, 2007. Female patient, 76 years of age, weighting 143.3 lb, was diagnosed with breast cancer and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, hypertension, osteoporosis, . ARIMIDEX dosage: unknown. During the same period patient was treated with ACTONEL, CALCIUM. Patient recovered.

Fosamax Side Effects Report #5475274-9
Physician from UNITED STATES reported FOSAMAX problem on Sept 25, 2007. Female patient, 72 years of age, weighting 224.9 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, hip fracture, . FOSAMAX dosage: unknown. During the same period patient was treated with AVALIDE, TOPROL, WARFARIN. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5475283-X
FOSAMAX problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 26, 2007. Female patient, 75 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, cardiac disorder, . FOSAMAX dosage: unknown. During the same period patient was treated with COREG, LIPITOR, NEXIUM, COZAAR. Patient recovered.

Clastoban Side Effects Report #5479155-6
Consumer or non-health professional from FRANCE reported CLASTOBAN problem on Oct 04, 2007. Female patient, 60 years of age, was diagnosed with breast cancer metastatic, metastases to bone and was treated with CLASTOBAN. After drug was administered, patient experienced the following problems/side effects: bone density decreased, bone disorder, dysphagia, facial neuralgia, infection, inflammation, mastication disorder, metastases to liver, . CLASTOBAN dosage: unknown. During the same period patient was treated with ZOMETA, TAXOTERE, XELODA, FORTIMEL, FEMARA, TAXOL. Patient died on 08/13/2003.

Evista Side Effects Report #5486908-7
EVISTA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 04, 2007. Female patient was diagnosed with osteoporosis and was treated with EVISTA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, . EVISTA dosage: 60 MG, UNK. Patient recovered.

Forteo Side Effects Report #5487131-2
Consumer or non-health professional from UNITED STATES reported FORTEO problem on Oct 04, 2007. Male patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: bone density decreased, cerebrovascular accident, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Arimidex Side Effects Report #5489368-5
ARIMIDEX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 10, 2007. Female patient, 68 years of age, weighting 173.9 lb, was diagnosed with breast cancer and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: bone density decreased, fatigue, gait disturbance, pain, . ARIMIDEX dosage: unknown. Patient recovered.

Zometa Side Effects Report #5492741-2
Consumer or non-health professional from FRANCE reported ZOMETA problem on Oct 15, 2007. Female patient, 81 years of age, was diagnosed with hypercalcaemia of malignancy and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: bone density decreased, osteonecrosis, pain in jaw, scintigraphy, . ZOMETA dosage: 4 MG, QMO. Patient was hospitalized and became disabled. Patient recovered.