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CALCINOSIS side effect

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Methylphenidate Side Effects Report #5669708-4
Physician from UNITED STATES reported METHYLPHENIDATE problem on Mar 07, 2008. Female patient, 20 years of age, was diagnosed with attention deficit/hyperactivity disorder, arthralgia and was treated with METHYLPHENIDATE. After drug was administered, patient experienced the following problems/side effects: calcinosis, laboratory test abnormal, livedo reticularis, skin disorder, skin ulcer, . METHYLPHENIDATE dosage: unknown. During the same period patient was treated with DEXTROAMPHETAMINE, LORATADINE, IBUPROFEN, CONTRACEPTIVES NOS, NAPROXEN. Patient recovered.

Omniscan Side Effects Report #5670088-9
OMNISCAN problem was reported by a Consumer or non-health professional from DENMARK on Feb 26, 2008. Male patient, 58 years of age, weighting 132.3 lb, was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, nephrogenic systemic fibrosis, renal failure, . OMNISCAN dosage: unknown. Patient recovered.

Prograf Side Effects Report #5674520-6
Physician from JAPAN reported PROGRAF problem on Feb 29, 2008. Female patient, 53 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: calcinosis, hydronephrosis, pyelonephritis, ureteral disorder, ureteric stenosis, . PROGRAF dosage: unknown. During the same period patient was treated with SIMULECT, METHYLPREDNISOLONE, MYCOPHENOLATE MOFETIL. Patient recovered.

Roaccutan Side Effects Report #5679345-3
ROACCUTAN problem was reported by a Physician from NORWAY on Mar 13, 2008. Female patient, 25 years of age, weighting 132.3 lb, was diagnosed with acne conglobata and was treated with ROACCUTAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, . ROACCUTAN dosage: unknown. Patient recovered.


Rituximab Side Effects Report #5684425-2
Consumer or non-health professional from UNITED KINGDOM reported RITUXIMAB problem on Mar 18, 2008. Female patient, weighting 140.0 lb, was diagnosed with b-cell lymphoma and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: calcinosis, carpal tunnel syndrome, crest syndrome, . RITUXIMAB dosage: 375 MG/M2, Q21D. During the same period patient was treated with ONCOVIN, ADRIAMYCIN PFS, ENDOXAN. Patient recovered.

Simulect Side Effects Report #5688676-2
SIMULECT problem was reported by a Consumer or non-health professional from JAPAN on Mar 25, 2008. Female patient, child 9 years of age, was diagnosed with renal transplant and was treated with SIMULECT. After drug was administered, patient experienced the following problems/side effects: calcinosis, cystitis bacterial, mucosal inflammation, pyuria, staphylococcal infection, therapeutic procedure, vesicoureteric reflux, . SIMULECT dosage: 20 MG, UNK. During the same period patient was treated with CYCLOSPORINE, CELLCEPT, METHYLPREDNISOLONE. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5689584-3
Consumer or non-health professional from UNITED STATES reported REBIF problem on Mar 18, 2008. Female patient, 50 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: calcinosis, dyspnoea, headache, ischaemia, . REBIF dosage: unknown. During the same period patient was treated with TOPAMAX, FIORICET. Patient recovered.

Magnevist Side Effects Report #5610959-2
MAGNEVIST problem was reported by a Physician from ITALY on Jan 11, 2008. Female patient, 66 years of age, was diagnosed with nuclear magnetic resonance imaging abdominal and was treated with MAGNEVIST. After drug was administered, patient experienced the following problems/side effects: calcinosis, gastrointestinal disorder, hypertensive crisis, malabsorption, mobility decreased, musculoskeletal stiffness, osteoarthritis, pain, . MAGNEVIST dosage: TOTAL DAILY DOSE: 40 ML. During the same period patient was treated with ERITROPOIETINA, MIMPARA. Patient recovered.

Humira Side Effects Report #5620487-6
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Jan 31, 2008. Female patient, weighting 159.1 lb, was diagnosed with psoriatic arthropathy, rheumatoid arthritis, cardiac disorder, stomach discomfort, hypothyroidism, seasonal allergy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: calcinosis, chest discomfort, sinusitis, . HUMIRA dosage: unknown. During the same period patient was treated with ASPIRIN, FAMOTIDINE, FEXOFENADINE, PRAVASTATIN, CLOPIDOGREL, LEVOTHYROXINE, FLUTICASONE PROPIONATE. Patient recovered.


Betamethasone Side Effects Report #5622963-9
BETAMETHASONE PHOSPHATE problem was reported by a Physician from JAPAN on Jan 25, 2008. Female patient, 85 years of age, was diagnosed with procedural site reaction and was treated with BETAMETHASONE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: calcinosis, graft complication, . BETAMETHASONE PHOSPHATE dosage: unknown. During the same period patient was treated with CRAVIT. Patient recovered.

Humira Side Effects Report #5623705-3
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 01, 2008. Female patient, weighting 159.1 lb, was diagnosed with psoriatic arthropathy, rheumatoid arthritis, cardiac disorder, stomach discomfort, hypothyroidism, seasonal allergy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: calcinosis, chest discomfort, sinusitis, . HUMIRA dosage: unknown. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, FAMOTIDINE, FEXOFENADINE, PRAVASTATIN, CLOPIDOGREL, LEVOTHYROXINE, FLUTICASONE PROPIONATE. Patient recovered.

Betamethasone Side Effects Report #5634211-4
BETAMETHASONE PHOSPHATE problem was reported by a Physician from JAPAN on Feb 06, 2008. Female patient, 85 years of age, was treated with BETAMETHASONE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: calcinosis, corneal deposits, nonspecific reaction, . BETAMETHASONE PHOSPHATE dosage: unknown. During the same period patient was treated with CRAVIT. Patient recovered.

Roaccutan Side Effects Report #5643129-2
Physician from FINLAND reported ROACCUTAN problem on Feb 15, 2008. Female patient, 60 years of age, was diagnosed with folliculitis and was treated with ROACCUTAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, eye disorder, polyneuropathy, . ROACCUTAN dosage: 10 MG EVERY OTHER DAY.. During the same period patient was treated with NITROFURANTOIN. Patient recovered.

Gamunex Side Effects Report #5649933-9
GAMUNEX problem was reported by a Physician from UNITED STATES on Feb 12, 2008. Female patient, 60 years of age, weighting 200.0 lb, was diagnosed with immunodeficiency common variable and was treated with GAMUNEX. After drug was administered, patient experienced the following problems/side effects: calcinosis, cardiac failure, pulmonary congestion, pulmonary embolism, pulmonary oedema, rotator cuff repair, thrombosis, thyroid neoplasm, . GAMUNEX dosage: unknown. During the same period patient was treated with ADVAIR DISKUS, ALLEGRA, THEOPHYLLINE, SINGULAIR, ACTONEL, ELMIRON, EVISTA, FOLIC ACID. Patient was hospitalized. Patient recovered.


Chantix Side Effects Report #5580736-X
Consumer or non-health professional from UNITED STATES reported CHANTIX problem on Dec 22, 2007. Male patient, weighting 140.3 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: calcinosis, myocardial infarction, stent placement, . CHANTIX dosage: unknown. Patient was hospitalized. Patient recovered.

Omniscan Side Effects Report #5588254-X
OMNISCAN problem was reported by a Consumer or non-health professional from JAPAN on Dec 25, 2007. Male patient, 53 years of age, weighting 125.7 lb, was diagnosed with acoustic neuroma, hydrocephalus and was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, grip strength decreased, haemodialysis, joint range of motion decreased, musculoskeletal stiffness, nephrogenic systemic fibrosis, . OMNISCAN dosage: unknown. Patient recovered.

Norvir Side Effects Report #5551616-0
Consumer or non-health professional from UNITED STATES reported NORVIR problem on Dec 06, 2007. Male patient, weighting 1.36 lb, was treated with NORVIR. After drug was administered, patient experienced the following problems/side effects: calcinosis, placental disorder, premature baby, . NORVIR dosage: unknown. During the same period patient was treated with ATAZANAVIR SULPHATE, EMTRICITABINE, TENOFOVIR DISOPROXIL FUMARATE. Patient died on 09/21/2007.

Forteo Side Effects Report #5518707-1
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 02, 2007. Female patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: calcinosis, gallbladder disorder, muscle spasms, pancreatitis, vitamin d decreased, . FORTEO dosage: unknown. During the same period patient was treated with CALCIUM. Patient was hospitalized. Patient recovered.

Cyclosporine Side Effects Report #5524724-8
Consumer or non-health professional from JAPAN reported CYCLOSPORINE problem on Nov 14, 2007. Female patient, child 9 years of age, was diagnosed with dermatomyositis and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: calcinosis, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with PREDNISOLONE, METHYLPREDNISOLONE, METHOTREXATE, IMMUNOGLOBULINS. Patient recovered.


Simulect Side Effects Report #5524931-4
SIMULECT problem was reported by a Consumer or non-health professional from JAPAN on Nov 16, 2007. Female patient, child 8 years of age, was diagnosed with renal transplant and was treated with SIMULECT. After drug was administered, patient experienced the following problems/side effects: calcinosis, cystitis bacterial, mucosal inflammation, pyuria, staphylococcal infection, therapeutic procedure, vesicoureteric reflux, . SIMULECT dosage: 20 MG, UNK. During the same period patient was treated with CYCLOSPORINE, CELLCEPT, METHYLPREDNISOLONE. Patient recovered.

Simulect Side Effects Report #5526211-X
Consumer or non-health professional from JAPAN reported SIMULECT problem on Nov 16, 2007. Female patient, child 8 years of age, was diagnosed with renal transplant and was treated with SIMULECT. After drug was administered, patient experienced the following problems/side effects: calcinosis, cystitis bacterial, mucosal inflammation, pyuria, staphylococcal infection, therapeutic procedure, vesicoureteric reflux, . SIMULECT dosage: 20 MG, UNK. During the same period patient was treated with CYCLOSPORINE, CELLCEPT, METHYLPREDNISOLONE. Patient recovered.

Cyclosporine Side Effects Report #5528666-3
CYCLOSPORINE problem was reported by a Consumer or non-health professional from JAPAN on Nov 22, 2007. Female patient, child 9 years of age, was diagnosed with dermatomyositis and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: calcinosis, . CYCLOSPORINE dosage: unknown. During the same period patient was treated with PREDNISOLONE, METHYLPREDNISOLONE, METHOTREXATE, IMMUNOGLOBULINS. Patient recovered.

Norvir Side Effects Report #5492551-6
Consumer or non-health professional from UNITED STATES reported NORVIR problem on Oct 15, 2007. Male patient, weighting 1.36 lb, was treated with NORVIR. After drug was administered, patient experienced the following problems/side effects: calcinosis, placental disorder, premature baby, . NORVIR dosage: unknown. During the same period patient was treated with ATAZANAVIR SULPHATE, EMTRICITABINE, TENOFOVIR DISOPROXIL FUMARATE. Patient died on 09/21/2007.

Avonex Side Effects Report #5504822-5
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 17, 2007. Male patient, 44 years of age, weighting 175.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: calcinosis, multiple sclerosis, spinal disorder, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Warfarin Side Effects Report #5448169-4
Health Professional from CZECH REPUBLIC reported WARFARIN problem on Aug 23, 2007. Female patient, 50 years of age, was diagnosed with coagulopathy and was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: calcinosis, extraskeletal ossification, haematoma, hysterectomy, muscle disorder, pelvic haemorrhage, pseudocyst, xanthoma, . WARFARIN dosage: unknown. Patient recovered.

Xopenex Side Effects Report #5409593-9
XOPENEX problem was reported by a Physician from UNITED STATES on July 25, 2007. Male patient, 76 years of age, weighting 177.0 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with XOPENEX. After drug was administered, patient experienced the following problems/side effects: calcinosis, dysphagia, foreign body trauma, haematocrit decreased, haemoglobin decreased, oesophageal discomfort, oesophageal food impaction, renal failure, spinal osteoarthritis, . XOPENEX dosage: unknown. During the same period patient was treated with SIMVASTATIN, LORCET, GEMFIBROZIL, TAMSULOSIN, PRINZIDE, CYANOCOBALAMIN, TYLENOL, PAROXETINE. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5442848-0
Consumer or non-health professional from UNITED STATES reported REBIF problem on Aug 16, 2007. Male patient, 52 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: calcinosis, dyspnoea, lymphadenopathy, pneumonia, pulmonary mass, . REBIF dosage: unknown. During the same period patient was treated with EXTRA STRENGTH TYLENOL, BENADRYL. Patient was hospitalized. Patient recovered.

Levoxyl Side Effects Report #5390578-6
LEVOXYL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 28, 2006. Female patient was diagnosed with thyroid disorder, hypertension, blood calcium decreased and was treated with LEVOXYL. After drug was administered, patient experienced the following problems/side effects: calcinosis, . LEVOXYL dosage: unknown. During the same period patient was treated with VASOTEC, CALCITRIOL. Patient recovered.

Rebif Side Effects Report #5392783-1
Consumer or non-health professional from UNITED KINGDOM reported REBIF problem on July 05, 2007. Female patient, 24 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: calcinosis, fat necrosis, injection site erythema, injection site macule, subcutaneous nodule, . REBIF dosage: unknown. Patient recovered.

Omniscan Side Effects Report #5401862-1
OMNISCAN problem was reported by a Consumer or non-health professional from JAPAN on July 18, 2007. Male patient, 53 years of age, weighting 125.7 lb, was diagnosed with acoustic neuroma and was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, gait disturbance, grip strength decreased, haemodialysis, joint range of motion decreased, nephrogenic systemic fibrosis, . OMNISCAN dosage: unknown. During the same period patient was treated with TAKEPRON OD, MARZULENE, CALCIUM, ISOSORBIDE DINITRATE, ETIZOLAM. Patient recovered.

Ascorbic Side Effects Report #5403282-2
Physician from UNITED STATES reported ASCORBIC ACID problem on July 27, 2007. Female patient, 49 years of age, was diagnosed with migraine and was treated with ASCORBIC ACID. After drug was administered, patient experienced the following problems/side effects: calcinosis, dehydration, haemodialysis, incorrect dose administered, orthostatic hypotension, oxalosis, renal failure acute, renal tubular necrosis, . ASCORBIC ACID dosage: unknown. During the same period patient was treated with IBUPROFEN. Patient was hospitalized. Patient recovered.

Levoxyl Side Effects Report #5390578-6
LEVOXYL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 28, 2006. Female patient was diagnosed with thyroid disorder, hypertension, blood calcium decreased and was treated with LEVOXYL. After drug was administered, patient experienced the following problems/side effects: calcinosis, . LEVOXYL dosage: unknown. During the same period patient was treated with VASOTEC, CALCITRIOL. Patient recovered.

Rebif Side Effects Report #5392783-1
Consumer or non-health professional from UNITED KINGDOM reported REBIF problem on July 05, 2007. Female patient, 24 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: calcinosis, fat necrosis, injection site erythema, injection site macule, subcutaneous nodule, . REBIF dosage: unknown. Patient recovered.

Omniscan Side Effects Report #5401862-1
OMNISCAN problem was reported by a Consumer or non-health professional from JAPAN on July 18, 2007. Male patient, 53 years of age, weighting 125.7 lb, was diagnosed with acoustic neuroma and was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, gait disturbance, grip strength decreased, haemodialysis, joint range of motion decreased, nephrogenic systemic fibrosis, . OMNISCAN dosage: unknown. During the same period patient was treated with TAKEPRON OD, MARZULENE, CALCIUM, ISOSORBIDE DINITRATE, ETIZOLAM. Patient recovered.

Ascorbic Side Effects Report #5403282-2
Physician from UNITED STATES reported ASCORBIC ACID problem on July 27, 2007. Female patient, 49 years of age, was diagnosed with migraine and was treated with ASCORBIC ACID. After drug was administered, patient experienced the following problems/side effects: calcinosis, dehydration, haemodialysis, incorrect dose administered, orthostatic hypotension, oxalosis, renal failure acute, renal tubular necrosis, . ASCORBIC ACID dosage: unknown. During the same period patient was treated with IBUPROFEN. Patient was hospitalized. Patient recovered.

Aredia Side Effects Report #5772264-3
AREDIA problem was reported by a Physician from GERMANY on June 03, 2008. Female patient was diagnosed with osteoporosis and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: calcinosis, condition aggravated, . AREDIA dosage: 60 MG, EVERY 3 MONTH. Patient recovered.

Humira Side Effects Report #5730740-3
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Apr 29, 2008. Male patient, weighting 195.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: calcinosis, scar, staphylococcal infection, streptococcal infection, . HUMIRA dosage: unknown. Patient recovered.

Boniva Side Effects Report #5705532-1
BONIVA problem was reported by a Consumer or non-health professional from POLAND on Apr 03, 2008. Female patient, weighting 114.6 lb, was diagnosed with osteoporosis postmenopausal, irritable bowel syndrome and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: calcinosis, pneumonitis, pulmonary calcification, . BONIVA dosage: unknown. During the same period patient was treated with FAMOGAST, DEBRIDAT, SECTRAL, TIALORID. Patient recovered.

Acitretin Side Effects Report #5345343-2
Physician from UNITED KINGDOM reported ACITRETIN problem on May 23, 2007. Male patient, 62 years of age, was diagnosed with psoriasis, pain and was treated with ACITRETIN. After drug was administered, patient experienced the following problems/side effects: calcinosis, constipation, dehydration, diarrhoea, eating disorder, enthesopathy, gastrointestinal disorder, impaired healing, . ACITRETIN dosage: unknown. During the same period patient was treated with MORPHINE, PARAFFIN, CAPASAL, BECLOMETHASONE DIPROPIONATE, SALBUTAMOL, OLANZAPINE, MIRTAZAPINE. Patient was hospitalized and became disabled. Patient recovered.

Comtan Side Effects Report #5353035-9
COMTAN problem was reported by a Consumer or non-health professional from FRANCE on May 18, 2007. Female patient, 78 years of age, was diagnosed with parkinson's disease and was treated with COMTAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, cholelithiasis, dehydration, disease progression, escherichia infection, flatulence, neuroleptic malignant syndrome, parkinson's disease, pyelonephritis, . COMTAN dosage: 800 MG. During the same period patient was treated with MODOPAR, LAROXYL, DEROXAT, EQUANIL, SERESTA. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5369594-6
Consumer or non-health professional from UNITED STATES reported REBIF problem on June 08, 2007. Male patient, 52 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: calcinosis, chest x-ray abnormal, condition aggravated, dyspnoea, lymphadenopathy, pneumonia, pulmonary mass, . REBIF dosage: unknown. During the same period patient was treated with EXTRA STRENGTH TYLENOL, BENADRYL. Patient was hospitalized. Patient recovered.

Karil Side Effects Report #5374351-0
KARIL problem was reported by a Physician from GERMANY on June 20, 2007. Female patient, weighting 156.5 lb, was diagnosed with osteoporosis and was treated with KARIL. After drug was administered, patient experienced the following problems/side effects: calcinosis, metaplasia, mucous membrane disorder, nasal cyst, rhinorrhoea, . KARIL dosage: unknown. Patient recovered.

Comtan Side Effects Report #5318762-8
Consumer or non-health professional from FRANCE reported COMTAN problem on Apr 10, 2007. Female patient, 78 years of age, was diagnosed with parkinson's disease and was treated with COMTAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, cholelithiasis, dehydration, disease progression, escherichia urinary tract infection, hypertonia, neuroleptic malignant syndrome, parkinson's disease, renal cyst, . COMTAN dosage: 800 MG; 800 MG. During the same period patient was treated with MODOPAR, LAROXYL, DEROXAT, EQUANIL, SERESTA. Patient was hospitalized. Patient recovered.

Tegretol Side Effects Report #5326910-9
TEGRETOL problem was reported by a Consumer or non-health professional from BRAZIL on Apr 26, 2007. Male patient, 18 years of age, was diagnosed with epilepsy, mental disorder and was treated with TEGRETOL. After drug was administered, patient experienced the following problems/side effects: calcinosis, gingival hyperplasia, neoplasm, . TEGRETOL dosage: 200 MG. During the same period patient was treated with HYDANTAL, GARDENAL. Patient recovered.

Forteo Side Effects Report #5338333-7
Physician from SPAIN reported FORTEO problem on May 16, 2007. Female patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: calcinosis, metrorrhagia, . FORTEO dosage: unknown. Patient recovered.

Rebif Side Effects Report #5346945-X
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on May 30, 2006. Female patient, 32 years of age, weighting 200.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: calcinosis, injection site erythema, soft tissue necrosis, . REBIF dosage: unknown. During the same period patient was treated with IBUPROFEN, TIZANIDINE, BACLOFEN, VERAPAMIL, MIDRIN. Patient was hospitalized. Patient recovered.

Xolair Side Effects Report #5289853-5
Consumer or non-health professional from UNITED STATES reported XOLAIR problem on Apr 03, 2007. Female patient, weighting 190.0 lb, was diagnosed with asthma and was treated with XOLAIR. After drug was administered, patient experienced the following problems/side effects: calcinosis, pain in extremity, . XOLAIR dosage: 375 MG, Q2W. During the same period patient was treated with ADVAIR DISKUS, NASAREL, SPIRIVA, ALBUTEROL, ATROVENT, ALLEGRA. Patient recovered.

Xolair Side Effects Report #5301146-6
XOLAIR problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 17, 2007. Female patient, weighting 190.0 lb, was diagnosed with asthma and was treated with XOLAIR. After drug was administered, patient experienced the following problems/side effects: calcinosis, pain in extremity, . XOLAIR dosage: 375 MG, Q2W. During the same period patient was treated with ADVAIR DISKUS, NASAREL, SPIRIVA, ALBUTEROL, ATROVENT, ALLEGRA. Patient recovered.

Forteo Side Effects Report #5308257-X
Consumer or non-health professional from UNITED STATES reported FORTEO problem on Apr 16, 2007. Female patient, 65 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: calcinosis, subcutaneous nodule, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Omniscan Side Effects Report #5313644-X
OMNISCAN problem was reported by a Consumer or non-health professional from JAPAN on Apr 13, 2007. Male patient, 24 years of age, weighting 136.7 lb, was diagnosed with malignant neoplasm of spinal cord and was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: calcinosis, disease progression, erythema, gait disturbance, haemodialysis, joint contracture, joint range of motion decreased, nephrogenic fibrosing dermopathy, pain of skin, . OMNISCAN dosage: 10 ML, SINGLE DOSE, I.V.. During the same period patient was treated with ALFACALCIDOL, PREDNISOLONE, LISINOPRIL, CLONAZEPAM, WASSER, AMLODIPINE BESYLATE, FERROUS SULPHATE, FAMOTIDINE. Patient recovered.

Erlotinib Side Effects Report #5314282-5
Health Professional from UNITED STATES reported ERLOTINIB problem on Apr 10, 2007. Female patient, 65 years of age, weighting 140.0 lb, was diagnosed with ovarian cancer and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: calcinosis, metastasis, nasal septum perforation, . ERLOTINIB dosage: 150 MG, ORAL. During the same period patient was treated with BEVACIZUMAB, LOTREL. Patient recovered.