Actonel and condition aggravated Patient Reports February 10, 2012

Actonel Side Effects Report #5008486-9
Actonel side effect was reported by a Physician from FRANCE on May 03, 2006. Female patient, 76 years of age, was diagnosed with osteoporosis prophylaxis, breast cancer  and was treated with Actonel. After drug was administered, patient experienced the following side effects: abdominal pain lower, adhesion , colonic atony, condition aggravated, constipation . Actonel dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with CALCIUM, VITAMIN D, ARIMIDEX. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5248058-4
Actonel side effect was reported by a Consumer or non-health professional from FRANCE on Feb 07, 2007. Female patient, 92 years of age, weighting 66.14 lb, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: cardiac failure, condition aggravated, dyspepsia. Actonel dosage: unknown. During the same period patient was treated with LASIX. Patient died.

Actonel Side Effects Report #4999851-4
Actonel side effect was reported by a Physician from GERMANY on May 03, 2006. Female patient, 82 years of age, weighting 154.3 lb, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, myasthenia gravis, unevaluable event. Actonel dosage: 70 MG, 1/WEEK, ORAL. During the same period patient was treated with MESTINON, CELLCEPT. Patient recovered.

Actonel Side Effects Report #5971945-6
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on Nov 10, 2008. Female patient, 80 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: back pain , condition aggravated, pain in extremity, vascular occlusion. Actonel dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with CALTRATE. Patient recovered.


Actonel Side Effects Report #4859938-3
Actonel side effect was reported by a Health Professional from UNITED KINGDOM on Dec 07, 2005. Female patient, 77 years of age, weighting 176.4 lb, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, headache , musculoskeletal stiffness, polymyalgia rheumatica . Actonel dosage: 35 MG, ORAL. During the same period patient was treated with PREDNISOLONE. Patient recovered.

Actonel Side Effects Report #5586155-4
Actonel side effect was reported by a Consumer or non-health professional from JAPAN on Dec 20, 2007. Female patient, 75 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, hepatic function abnormal, hyperkalaemia. Actonel dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with LOXONIN, MYONAL, ETODOLAC, NEUROTROPIN, MAGMITT, LANSOPRAZOLE, GASTROM. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5615211-7
Actonel side effect was reported by a Physician from JAPAN on Jan 16, 2008. Female patient, 75 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: blood creatinine increased, blood urea increased, condition aggravated, hepatic function abnormal, hyperkalaemia, metabolic acidosis. Actonel dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with LOXONIN, VOLTAREN, MYONAL. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5878583-4
Actonel side effect was reported by a Physician from CANADA on Aug 26, 2008. Female patient, 75 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, eczema , leukocytoclastic vasculitis, pneumonia pneumococcal. Actonel dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with TYLENOL, EFFEXOR. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5099930-X
Actonel side effect was reported by a Health Professional from FRANCE on Aug 23, 2006. Female patient, 74 years of age, was diagnosed with osteoporosis , cystitis, hypovitaminosis and was treated with Actonel. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, c-reactive protein increased, condition aggravated, cyanosis, dermatomyositis, pain in extremity, raynaud's phenomenon, rhabdomyolysis. Actonel dosage: 35 MG, 1/WEEK, ORAL. During the same period patient was treated with ENOXOR, IDEOS. Patient was hospitalized. Patient recovered.


Actonel Side Effects Report #4816140-9
Actonel side effect was reported by a Pharmacist from UNITED STATES on Oct 14, 2005. Female patient, 74 years of age, weighting 130.1 lb, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, impaired driving ability. Actonel dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with LISINOPRIL, ATENOLOL, PREMARIN, MEDROXYPROGESTERONE, BETIMOL, TYLENOL. Patient recovered.

Actonel Side Effects Report #5361355-7
Actonel side effect was reported by a Physician from LITHUANIA on June 05, 2007. Female patient, 73 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, groin pain, osteonecrosis , radiculopathy. Actonel dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with VITAMIN B. Patient recovered.

Actonel Side Effects Report #5020724-5
Actonel side effect was reported by a Physician from JAPAN on May 17, 2006. Female patient, 73 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, dysphagia, liver disorder, oesophageal stenosis, pharyngitis. Actonel dosage: 2.5 MG DAILY, ORAL. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5409371-0
Actonel side effect was reported by a Consumer or non-health professional from AUSTRALIA on July 25, 2007. Female patient, 71 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, renal failure. Actonel dosage: 35 MG, ORAL. During the same period patient was treated with AVAPRO HCT, TAZAC. Patient recovered.

Actonel Side Effects Report #6140642-9
Actonel side effect was reported by a Physician from CANADA on Mar 17, 2009. Female patient, 70 years of age, was diagnosed with osteoporosis , cardiovascular event prophylaxis and was treated with Actonel. After drug was administered, patient experienced the following side effects: activated partial thromboplastin time prolonged, angina unstable, blood creatine phosphokinase increased, blood creatinine increased, blood potassium increased, blood pressure systolic increased, chest discomfort, condition aggravated, constipation . Actonel dosage: 35MG ONCE WEEKLY, ORAL. During the same period patient was treated with ACETYLSALICYLIC ACID SRT, IRBESARTAN, ALTACE, FIBRATES, ORAL ANTIDIABETICS, METFORMIN, NOVOLIN. Patient was hospitalized. Patient recovered.


Actonel Side Effects Report #5739882-X
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on May 13, 2008. Female patient, 68 years of age, weighting 147.0 lb, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: back disorder, condition aggravated, musculoskeletal pain. Actonel dosage: unknown. Patient recovered.

Actonel Side Effects Report #4745065-2
Actonel side effect was reported by a Health Professional from UNITED STATES on Aug 02, 2005. Female patient, 65 years of age, weighting 162.9 lb, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: bone disorder, condition aggravated, dyspepsia, eye infection , haemoglobin decreased, jaw disorder, post procedural haemorrhage, swelling face. Actonel dosage: 30 MG ONCE WEEKLY, ORAL. During the same period patient was treated with ACIPHEX, LESCOL, CALCIUM, DARVOCET. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5763472-6
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 04, 2007. Female patient, 61 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: bone disorder, condition aggravated, dental caries, dental discomfort, ear pain, erythema, gingival recession, gingivitis, mouth ulceration. Actonel dosage: unknown. During the same period patient was treated with FOSAMAX, VIOXX, COVERA, LIPITOR, CHEMDEC DM, CITALOPRAM HYDROBROMIDE, EFFEXOR, IBUPROFEN. Patient recovered.

Actonel Side Effects Report #5023426-4
Actonel side effect was reported by a Physician from JAPAN on May 19, 2006. Female patient, 54 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, arthritis , aspartate aminotransferase increased, condition aggravated, liver disorder. Actonel dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with PREDNISOLONE, FLUCAM. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #4998431-4
Actonel side effect was reported by a Consumer or non-health professional from JAPAN on Apr 27, 2006. Female patient, 53 years of age, weighting 80.47 lb, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: autoimmune hepatitis, cholestasis, condition aggravated, fatigue, hepatic fibrosis, hepatocellular damage, hypertrophy, liver disorder. Actonel dosage: 2.5 MG DAILY, ORAL. Patient was hospitalized. Patient recovered.


Actonel Side Effects Report #5818977-6
Actonel side effect was reported by a Physician from JAPAN on July 07, 2008. Female patient, 36 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, skin ulcer. Actonel dosage: 2.5 MG, ORAL. Patient recovered.

Actonel Side Effects Report #5846268-6
Actonel side effect was reported by a Physician from JAPAN on July 29, 2008. Female patient, 36 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, skin ulcer. Actonel dosage: 17.5 MG, 1 /WEEK, ORAL. During the same period patient was treated with PREDONINE, WARFARIN POTASSIUM, ASPIRIN, ANPLAG, RABEPRAZOLE, JUVELA N, FERROMIA, PRIMPERAN. Patient recovered.

Actonel Side Effects Report #5199502-2
Actonel side effect was reported by a Physician from JAPAN on Dec 20, 2006. Female patient, 21 years of age, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, haemoglobin decreased, platelet count decreased, red blood cell abnormality, systemic lupus erythematosus, thrombotic thrombocytopenic purpura. Actonel dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with PREDONINE, PERSANTIN, SUCRALFATE, CEFDINIR, LOSARTAN POTASSIUM, BREDININ. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5376537-8
Actonel side effect was reported by a Physician from SOUTH AFRICA on June 20, 2007. Female patient was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, epilepsy . Actonel dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with TOPAMAX, LAMICTAL, GEODON, DISPRIN. Patient recovered.

Actonel Side Effects Report #4703043-3
Actonel side effect was reported by a Consumer or non-health professional from on June 28, 2005. Female patient, weighting 165.0 lb, was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: activities of daily living impaired, condition aggravated, osteoporosis , polymyalgia rheumatica . Actonel dosage: unknown. Patient recovered.


Actonel Side Effects Report #4816224-5
Actonel side effect was reported by a Physician from GERMANY on Oct 19, 2005. Female patient was diagnosed with osteoporosis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: blood calcium increased, condition aggravated. Actonel dosage: unknown. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5008907-1
Actonel side effect was reported by a Physician from UNITED STATES on May 03, 2006. Female patient, 63 years of age, weighting 162.0 lb, was diagnosed with osteopenia, arthritis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: abdominal pain upper, anxiety , arthralgia, back pain , condition aggravated, depression , diarrhoea, dislocation of joint prosthesis. Actonel dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with VICODIN ES, VICODIN ES, VICODIN ES, BEXTRA, ALPRAZOLAM, KEFLEX, LEXAPRO. Patient recovered.

Actonel Side Effects Report #5662886-2
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 11, 2008. Female patient, 58 years of age, weighting 123.0 lb, was diagnosed with osteopenia, spinal column stenosis and was treated with Actonel. After drug was administered, patient experienced the following side effects: bone pain, condition aggravated, fibromyalgia. Actonel dosage: 35 MG-1 TABLET- WEEKLY PO. Patient recovered.

Actonel Side Effects Report #5409437-5
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 08, 2007. Female patient, 55 years of age, weighting 120.0 lb, was diagnosed with osteopenia and was treated with Actonel. After drug was administered, patient experienced the following side effects: arthralgia, bone pain, condition aggravated, osteopenia, osteoporosis . Actonel dosage: 35 MG ONCE A WEEK PO. Patient recovered.

Actonel Side Effects Report #4734566-9
Actonel side effect was reported by a Health Professional from UNITED STATES on July 19, 2005. Female patient, 65 years of age, was diagnosed with bone disorder and was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, dyspepsia, haemoglobin decreased, post procedural haemorrhage. Actonel dosage: 30 MG ONCE WEEKLY, ORAL. During the same period patient was treated with ACIPHEX, LESCOL. Patient was hospitalized. Patient recovered.


Actonel Side Effects Report #5064827-8
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on July 18, 2006. Female patient was diagnosed with bone density decreased and was treated with Actonel. After drug was administered, patient experienced the following side effects: asthma , condition aggravated, dyspnoea, respiratory tract infection. Actonel dosage: unknown. During the same period patient was treated with CLUCOCORTICOSTEROIDS INHALER. Patient recovered.

Actonel Side Effects Report #5795359-7
Actonel side effect was reported by a Health Professional from UNITED STATES on June 11, 2008. Female patient, 65 years of age, weighting 132.1 lb, was diagnosed with back pain  and was treated with Actonel. After drug was administered, patient experienced the following side effects: back pain , bone marrow disorder, bone marrow tumour cell infiltration, condition aggravated, neoplasm malignant. Actonel dosage: 35 MG, 1 /WEEK, ORAL. During the same period patient was treated with TOPROL, TAMOXIFEN CITRATE, CLONIDINE, FLEXERIL, ASPIRIN, TRAZODONE, COMBIVENT. Patient recovered.

Actonel Side Effects Report #5808281-4
Actonel side effect was reported by a Health Professional from UNITED STATES on June 26, 2008. Female patient, 65 years of age, weighting 132.1 lb, was diagnosed with back pain  and was treated with Actonel. After drug was administered, patient experienced the following side effects: back pain , bone marrow tumour cell infiltration, condition aggravated, cyst, metastases to bone, multiple myeloma , myelodysplastic syndrome, osteopenia, spinal compression fracture. Actonel dosage: 35 MG, 1 /WEEK, ORAL. During the same period patient was treated with TOPROL, TAMOXIFEN CITRATE, CLONIDINE, FLEXERIL, ASPIRIN, TRAZODONE, COMBIVENT. Patient recovered.

Actonel Side Effects Report #5940631-0
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on Nov 03, 2008. Male patient, weighting 150.0 lb, was diagnosed with arthritis  and was treated with Actonel. After drug was administered, patient experienced the following side effects: arthralgia, condition aggravated, diarrhoea, gastrooesophageal reflux disease, influenza like illness, joint swelling, myalgia, neck pain. Actonel dosage: 150MG. 1 A MO (1). During the same period patient was treated with NAPROXEN. Patient recovered.

Actonel Side Effects Report #5689911-7
Actonel side effect was reported by a Pharmacist from UNITED STATES on Mar 31, 2008. Female patient, 80 years of age, was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, oral torus. Actonel dosage: 35MG WEEKLY PO. Patient recovered.


Actonel Side Effects Report #6062566-8
Actonel side effect was reported by a Physician from AUSTRALIA on Jan 15, 2009. Female patient, 75 years of age, was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, gastrooesophageal reflux disease, malaise. Actonel dosage: unknown. During the same period patient was treated with NEXIUM, MOTILIUM, CELEBREX, ADALAT, NORVASC, ASPIRIN. Patient recovered.

Actonel Side Effects Report #4616370-5
Actonel side effect was reported by a Pharmacist from on Mar 07, 2005. Female patient, 73 years of age, was treated with Actonel. After drug was administered, patient experienced the following side effects: arthralgia, arthritis , condition aggravated, difficulty in walking. Actonel dosage: 35 MG ONCE WEEKLY, ORAL. Patient recovered.

Actonel Side Effects Report #5979424-7
Actonel side effect was reported by a Physician from GREECE on Nov 13, 2008. Female patient, 67 years of age, was treated with Actonel. After drug was administered, patient experienced the following side effects: atrial fibrillation , condition aggravated. Actonel dosage: unknown. Patient recovered.

Actonel Side Effects Report #5084754-X
Actonel side effect was reported by a Health Professional from FRANCE on Aug 03, 2006. Female patient, 65 years of age, weighting 110.2 lb, was treated with Actonel. After drug was administered, patient experienced the following side effects: alopecia, arthralgia, condition aggravated, rheumatoid arthritis , scleritis, synovitis, visual acuity reduced. Actonel dosage: unknown. During the same period patient was treated with ARAVA, ENBREL, PREDNISONE, SULFASALAZINE. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5944759-0
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 22, 2008. Female patient, 65 years of age, was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, diplopia, eye pain, eyelid ptosis, facial palsy, lung neoplasm, lung neoplasm malignant, ocular hyperaemia. Actonel dosage: 150 MG ONCE MONTHLY, ORAL. During the same period patient was treated with CALCIUM, VITAMIN D, PLAVIX, ASPIRIN. Patient was hospitalized. Patient recovered.


Actonel Side Effects Report #5849393-9
Actonel side effect was reported by a Physician from UNITED STATES on Aug 08, 2008. Female patient, 57 years of age, was treated with Actonel. After drug was administered, patient experienced the following side effects: abasia, arthralgia, arthritis , bone pain, condition aggravated, gastrooesophageal reflux disease, hypophagia, pyrexia. Actonel dosage: 150 MG, ORAL. Patient recovered.

Actonel Side Effects Report #5762006-X
Actonel side effect was reported by a Physician from GREECE on May 22, 2008. Female patient, 36 years of age, was treated with Actonel. After drug was administered, patient experienced the following side effects: condition aggravated, nephrolithiasis. Actonel dosage: 35 MG, 1 /WEEK, ORAL. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5452764-6
Actonel side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 21, 2007. Female patient was diagnosed with systemic lupus erythematosus and was treated with Actonel. After drug was administered, patient experienced the following side effects: alopecia, condition aggravated, oral disorder, sjogren's syndrome . Actonel dosage: unknown. During the same period patient was treated with ROZEREM, CELLCEPT, PLAQUENIL. Patient recovered.