Risedronate and condition aggravated Patient Reports February 12, 2012

Risedronate Side Effects Report #5995084-3
Risedronate side effect was reported by a Physician from JAPAN on Nov 25, 2008. Male patient, 83 years of age, was diagnosed with osteoporosis prophylaxis and was treated with Risedronate. After drug was administered, patient experienced the following side effects: condition aggravated, gingival disorder, injury, oral torus, stomatitis. Risedronate dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with PREDONINE. Patient recovered.

Risedronate Side Effects Report #4704681-4
Risedronate side effect was reported by a Physician from on June 16, 2005. Female patient, 93 years of age, weighting 97.44 lb, was diagnosed with osteoporosis  and was treated with Risedronate. After drug was administered, patient experienced the following side effects: cardiac failure, condition aggravated, marasmus. Risedronate dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with LORCAM, ARTZ, XYLOCAINE, LIDOCAINE HYDROCHLORIDE, BETAMETHASONE, NORVASC, DEKASOFT, NITRODERM. Patient was hospitalized. Patient recovered.

Risedronate Side Effects Report #5673101-8
Risedronate side effect was reported by a Physician from JAPAN on Mar 03, 2008. Female patient, 81 years of age, was diagnosed with osteoporosis , rheumatoid arthritis  and was treated with Risedronate. After drug was administered, patient experienced the following side effects: condition aggravated, osteolysis, osteomyelitis, rheumatoid arthritis , skin ulcer. Risedronate dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with RHEUMATREX, PREDNISOLONE, CORTICOSTEROIDS, MOBIC, LANSOPRAZOLE, VIT K CAP, ASPARA. Patient was hospitalized. Patient recovered.

Risedronate Side Effects Report #5401426-X
Risedronate side effect was reported by a Physician from JAPAN on July 13, 2007. Female patient, 77 years of age, was diagnosed with osteoporosis  and was treated with Risedronate. After drug was administered, patient experienced the following side effects: cholelithiasis, condition aggravated, hypertension, shock. Risedronate dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with LOXONIN, MUCOSTA, MOBIC, IRGAS. Patient was hospitalized. Patient recovered.


Risedronate Side Effects Report #5786746-1
Risedronate side effect was reported by a Health Professional from JAPAN on June 04, 2008. Female patient, 62 years of age, was diagnosed with osteoporosis , rheumatoid arthritis  and was treated with Risedronate. After drug was administered, patient experienced the following side effects: condition aggravated, leukopenia, urticaria. Risedronate dosage: 2.5 MG ONCE DAILY, ORAL; 2.5 MG ONCE DAILY, ORAL. During the same period patient was treated with CELECOXIB, LANSOPRAZOLE, MEDROL, ZOLPIDEM TARTRATE, ONEALFA, MUCOSTA. Patient recovered.

Risedronate Side Effects Report #5818980-6
Risedronate side effect was reported by a Health Professional from JAPAN on July 02, 2008. Female patient, 62 years of age, was diagnosed with osteoporosis , rheumatoid arthritis  and was treated with Risedronate. After drug was administered, patient experienced the following side effects: condition aggravated, discomfort, leukopenia, pain , urticaria. Risedronate dosage: 2.5 MG ONCE DAILY, ORAL; 2.5 MG ONCE DAILY, ORAL. During the same period patient was treated with CELECOXIB, LANSOPRAZOLE, MEDROL, ZOLPIDEM TARTRATE, ONEALFA, MUCOSTA, RIMATIL. Patient was hospitalized. Patient recovered.

Risedronate Side Effects Report #5357153-0
Risedronate side effect was reported by a Physician from JAPAN on May 30, 2007. Female patient, 54 years of age, was diagnosed with osteoporosis  and was treated with Risedronate. After drug was administered, patient experienced the following side effects: condition aggravated, diabetes mellitus, treatment noncompliance. Risedronate dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with PELETON, NATEGLINIDE, AMARYL, NEOPHAGEN, MOHRUS, NEO VITACAIN. Patient was hospitalized. Patient recovered.

Risedronate Side Effects Report #5159320-8
Risedronate side effect was reported by a Physician from JAPAN on Nov 07, 2006. Female patient, 35 years of age, was diagnosed with osteoporosis  and was treated with Risedronate. After drug was administered, patient experienced the following side effects: basophil count decreased, blood alkaline phosphatase increased, blood creatinine decreased, condition aggravated, eosinophil count decreased, granulocytopenia, lymphocyte count increased, monocyte count increased, neutrophil count decreased. Risedronate dosage: 2.5 MG DAILY, ORAL. During the same period patient was treated with BONALON, FAMOTIDINE, PREDNISOLONE, SULFAMETHOXAZOLE, ALFAROL, PERSANTIN. Patient recovered.

Risedronate Side Effects Report #4546558-3
Risedronate side effect was reported by a Health Professional from on Dec 21, 2004. Female patient was diagnosed with osteoporosis  and was treated with Risedronate. After drug was administered, patient experienced the following side effects: blepharitis, cataract , condition aggravated, conjunctivitis, corneal deposits, corneal ulcer, diplopia. Risedronate dosage: unknown. Patient recovered.