PATHOLOGICAL FRACTURE side effect
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Drugs associated with PATHOLOGICAL FRACTURE
ACTOS AMARYL AREDIA ATRIPLA AVANDAMET AVANDIA BEVACIZUMAB CEREZYME CRIXIVAN DURAGESIC FLUDEX FORTEO FOSAMAX GLUCOPHAGE HEPSERA HUMIRA LIORESAL NEXAVAR PREDNISONE REMICADE RESCRIPTOR REVLIMID RIFABUTIN TEMSIROLIMUS THALOMID TOPOTECAN VIANI VIREAD ZOMETABevacizumab Side Effects Report #5618810-1
Physician from UNITED KINGDOM reported BEVACIZUMAB problem on Jan 23, 2008. Male patient was diagnosed with colon cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . BEVACIZUMAB dosage: 5 MG/KG, UNK. During the same period patient was treated with OXALIPLATIN, FLUOROURACIL, ISOVORIN, IRINOTECAN, ACTOS, BLOPRESS, LOXONIN. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5597655-5
HUMIRA problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Jan 11, 2008. Female patient, weighting 123.5 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: pathological fracture, post procedural infection, sepsis, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, PREDNISOLONE, ACETAMINOPHEN W, ESOMEPRAZOLE, FOLIC ACID, NABUMETONE. Patient died on 06/30/2007.
Revlimid Side Effects Report #5613421-6
Physician from UNITED STATES reported REVLIMID problem on Jan 21, 2008. Female patient, 63 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . REVLIMID dosage: 25 MG, 1 IN 1 D, ORAL. Patient was hospitalized. Patient recovered.
Glucophage Side Effects Report #5513948-1
GLUCOPHAGE problem was reported by a Health Professional from GERMANY on Nov 02, 2007. Female patient, 68 years of age, was diagnosed with type 2 diabetes mellitus, dyslipidaemia and was treated with GLUCOPHAGE. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . GLUCOPHAGE dosage: unknown. During the same period patient was treated with ACTOS, AMARYL, ZOCOR, ACUITEL, INDAPAMIDE, BACLOFEN, MYOLASTAN, AMPECYCLAL. Patient recovered.
Amaryl Side Effects Report #5515891-0
Consumer or non-health professional from reported AMARYL problem on Nov 05, 2007. Female patient, 68 years of age, was treated with AMARYL. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . AMARYL dosage: unknown. During the same period patient was treated with ACTOS, GLUCOPHAGE, ZOCOR, ACUITEL, INDAPAMIDE, LIORESAL, MYOLASTAN, AMPECYCLAL. Patient recovered.
Fludex Side Effects Report #5517386-7
FLUDEX problem was reported by a Consumer or non-health professional from FRANCE on Nov 08, 2007. Female patient was diagnosed with dyslipidaemia and was treated with FLUDEX. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . FLUDEX dosage: unknown. During the same period patient was treated with ACTOS, AMARYL, GLUCOPHAGE, ZOCOR, ACUITEL, LIORESAL, MYOLASTAN, AMPECYCLAL. Patient recovered.
Glucophage Side Effects Report #5525214-9
Health Professional from GERMANY reported GLUCOPHAGE problem on Nov 19, 2007. Female patient, 68 years of age, was diagnosed with type 2 diabetes mellitus, dyslipidaemia and was treated with GLUCOPHAGE. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . GLUCOPHAGE dosage: unknown. During the same period patient was treated with ACTOS, AMARYL, ZOCOR, ACUITEL, FLUDEX, BACLOFEN, MYOLASTAN, AMPECYCLAL. Patient recovered.
Lioresal Side Effects Report #5527793-4
LIORESAL problem was reported by a Consumer or non-health professional from FRANCE on Nov 22, 2007. Female patient was diagnosed with diabetes mellitus, dyslipidaemia and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . LIORESAL dosage: unknown. During the same period patient was treated with ACTOS, AMARYL, GLUCOPHAGE, ZOCOR, ACUITEL, FLUDEX, MYOLASTAN, AMPECYCLAL. Patient recovered.
Humira Side Effects Report #5530870-5
Consumer or non-health professional from UNITED KINGDOM reported HUMIRA problem on Nov 27, 2007. Female patient, weighting 123.5 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: pathological fracture, post procedural infection, sepsis, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, PREDNISOLONE, ACETAMINOPHEN W, ESOMEPRAZOLE, FOLIC ACID, NABUMETONE. Patient died on 06/30/2007.
Avandia Side Effects Report #5492011-2
AVANDIA problem was reported by a Consumer or non-health professional from NETHERLANDS on Oct 15, 2007. Female patient, 44 years of age, weighting 253.5 lb, was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: pathological fracture, wrist fracture, . AVANDIA dosage: 4MG PER DAY. Patient recovered.
Actos Side Effects Report #5497860-2
Consumer or non-health professional from GERMANY reported ACTOS problem on Oct 17, 2007. Female patient was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . ACTOS dosage: unknown. Patient recovered.
Actos Side Effects Report #5504304-0
ACTOS problem was reported by a Consumer or non-health professional from SPAIN on Oct 24, 2007. Female patient, 54 years of age, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . ACTOS dosage: 45 MG, PER ORAL. Patient recovered.
Thalomid Side Effects Report #5449896-5
Physician from UNITED STATES reported THALOMID problem on Aug 31, 2007. Female patient, 81 years of age, was diagnosed with gammopathy and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . THALOMID dosage: unknown. Patient was hospitalized. Patient died on 07/19/2007.
Avandamet Side Effects Report #5377410-1
AVANDAMET problem was reported by a Consumer or non-health professional from IRELAND on June 26, 2007. Female patient, 58 years of age, was diagnosed with diabetes mellitus and was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . AVANDAMET dosage: unknown. During the same period patient was treated with LIPITOR, ASPIRIN, DIAMICRON, CALCICHEW, FORTEO. Patient recovered.
Temsirolimus Side Effects Report #5385602-0
Physician from UNITED STATES reported TEMSIROLIMUS problem on July 03, 2007. Male patient, weighting 180.8 lb, was diagnosed with renal cell carcinoma stage iv, hypersensitivity, oedema, reflux oesophagitis, nausea, flatulence, constipation, insomnia and was treated with TEMSIROLIMUS. After drug was administered, patient experienced the following problems/side effects: pathological fracture, rectal haemorrhage, . TEMSIROLIMUS dosage: unknown. During the same period patient was treated with OPTICRON, FUROSEMIDE, OMEPRAZOLE, COMPAZINE, DIMETICONE, DOCUSATE, TEMAZEPAM, POTASSIUM ACETATE. Patient was hospitalized. Patient recovered.
Bevacizumab Side Effects Report #5391779-3
BEVACIZUMAB problem was reported by a Physician from UNITED KINGDOM on July 05, 2007. Female patient was diagnosed with breast cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . BEVACIZUMAB dosage: 880 MG, DAYS 1+15. During the same period patient was treated with CAELYX, NIFEDIPINE, METOPROLOL SUCCINATE, HYDROCHLOROTHIAZIDUM, ASPIRIN, PHENYTOIN. Patient was hospitalized. Patient recovered.
Remicade Side Effects Report #5399778-2
Pharmacist from CANADA reported REMICADE problem on July 17, 2007. Female patient, 50 years of age, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . REMICADE dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient recovered.
Avandamet Side Effects Report #5377410-1
AVANDAMET problem was reported by a Consumer or non-health professional from IRELAND on June 26, 2007. Female patient, 58 years of age, was diagnosed with diabetes mellitus and was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . AVANDAMET dosage: unknown. During the same period patient was treated with LIPITOR, ASPIRIN, DIAMICRON, CALCICHEW, FORTEO. Patient recovered.
Temsirolimus Side Effects Report #5385602-0
Physician from UNITED STATES reported TEMSIROLIMUS problem on July 03, 2007. Male patient, weighting 180.8 lb, was diagnosed with renal cell carcinoma stage iv, hypersensitivity, oedema, reflux oesophagitis, nausea, flatulence, constipation, insomnia and was treated with TEMSIROLIMUS. After drug was administered, patient experienced the following problems/side effects: pathological fracture, rectal haemorrhage, . TEMSIROLIMUS dosage: unknown. During the same period patient was treated with OPTICRON, FUROSEMIDE, OMEPRAZOLE, COMPAZINE, DIMETICONE, DOCUSATE, TEMAZEPAM, POTASSIUM ACETATE. Patient was hospitalized. Patient recovered.
Bevacizumab Side Effects Report #5391779-3
BEVACIZUMAB problem was reported by a Physician from UNITED KINGDOM on July 05, 2007. Female patient was diagnosed with breast cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . BEVACIZUMAB dosage: 880 MG, DAYS 1+15. During the same period patient was treated with CAELYX, NIFEDIPINE, METOPROLOL SUCCINATE, HYDROCHLOROTHIAZIDUM, ASPIRIN, PHENYTOIN. Patient was hospitalized. Patient recovered.
Remicade Side Effects Report #5399778-2
Pharmacist from CANADA reported REMICADE problem on July 17, 2007. Female patient, 50 years of age, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . REMICADE dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient recovered.
Revlimid Side Effects Report #5756498-X
REVLIMID problem was reported by a Physician from UNITED STATES on May 19, 2008. Female patient, 63 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . REVLIMID dosage: 25 MG, 1 IN 1 D, ORAL. Patient was hospitalized. Patient recovered.
Bevacizumab Side Effects Report #5703405-1
Physician from UNITED KINGDOM reported BEVACIZUMAB problem on Mar 28, 2008. Male patient was diagnosed with colon cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . BEVACIZUMAB dosage: 5 MG/KG, UNK. During the same period patient was treated with OXALIPLATIN, FLUOROURACIL, ISOVORIN, IRINOTECAN HYDROCHLORIDE, ACTOS, BLOPRESS, LOXONIN. Patient was hospitalized. Patient died on 02/05/2008.
Avandia Side Effects Report #5345955-6
AVANDIA problem was reported by a Consumer or non-health professional from SPAIN on June 01, 2007. Female patient, 64 years of age, weighting 220.5 lb, was diagnosed with diabetes mellitus and was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . AVANDIA dosage: 8MG PER DAY. Patient recovered.
Avandia Side Effects Report #5332381-9
Consumer or non-health professional from IRELAND reported AVANDIA problem on May 15, 2007. Female patient, 58 years of age, was diagnosed with diabetes mellitus and was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: pathological fracture, . AVANDIA dosage: unknown. During the same period patient was treated with AVANDAMET, LIPITOR, ASPIRIN, DIAMICRON, CALCICHEW, FORTEO. Patient recovered.
Revlimid Side Effects Report #5678390-1
REVLIMID problem was reported by a Physician from NETHERLANDS on Mar 13, 2008. Female patient, 66 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: humerus fracture, pathological fracture, . REVLIMID dosage: 15 MG, 2 IN 1 D, ORAL; 25 MG, 1 IN 1 D, ORAL. Patient was hospitalized. Patient recovered.
Aredia Side Effects Report #5621779-7
Consumer or non-health professional from GERMANY reported AREDIA problem on Feb 07, 2008. Male patient was diagnosed with plasmacytoma and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: impaired healing, pathological fracture, . AREDIA dosage: 90 MG, QMO. Patient recovered.
Fosamax Side Effects Report #5626872-0
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 08, 2008. Female patient, 79 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: femur fracture, pathological fracture, . FOSAMAX dosage: unknown. During the same period patient was treated with PREDNISONE. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5628363-X
Physician from NETHERLANDS reported HUMIRA problem on Feb 07, 2008. Male patient, weighting 198.4 lb, was diagnosed with psoriatic arthropathy, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: haemothorax, pathological fracture, rib fracture, . HUMIRA dosage: unknown. During the same period patient was treated with FOSINOPRIL, METHOTREXATE. Patient was hospitalized. Patient recovered.
Rifabutin Side Effects Report #5633564-0
RIFABUTIN problem was reported by a Consumer or non-health professional from NEW ZEALAND on Feb 11, 2008. Male patient, 59 years of age, was diagnosed with mycobacterium avium complex infection and was treated with RIFABUTIN. After drug was administered, patient experienced the following problems/side effects: osteomalacia, pathological fracture, vitamin d deficiency, . RIFABUTIN dosage: unknown. During the same period patient was treated with ZIDOVUDINE, LAMIVUDINE, INDINIVIR SULPHATE, RITONAVIR, CIPROFLOXACIN, ETHAMBUTOL HYDROCHLORIDE. Patient recovered.
Fosamax Side Effects Report #5505404-1
Health Professional from JAPAN reported FOSAMAX problem on Oct 26, 2007. Female patient, 78 years of age, weighting 85.98 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: low turnover osteopathy, pathological fracture, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Actos Side Effects Report #5522888-3
ACTOS problem was reported by a Consumer or non-health professional from GERMANY on Nov 08, 2007. Female patient, 50 years of age, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: foot fracture, pathological fracture, . ACTOS dosage: 15 M G (15 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with ALLOPURINOL, METFORMIN, ENALAPRIL MALEATE, ACETYLSALICYLIC ACID SRT. Patient recovered.
Fosamax Side Effects Report #5526079-1
Health Professional from JAPAN reported FOSAMAX problem on Nov 16, 2007. Female patient, 78 years of age, weighting 85.98 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: low turnover osteopathy, pathological fracture, . FOSAMAX dosage: unknown. During the same period patient was treated with LIPITOR, CYANOCOBALAMIN, SERMION, ALINAMIN F, CEROCRAL, LENDORMIN, MAGNESIUM OXIDE, LORAZEPAM. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5484392-0
FOSAMAX problem was reported by a Health Professional from JAPAN on Sept 28, 2007. Female patient, 78 years of age, weighting 85.98 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: low turnover osteopathy, pathological fracture, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Rescriptor Side Effects Report #5484514-1
Health Professional from CANADA reported RESCRIPTOR problem on Oct 03, 2007. Male patient, weighting 208.1 lb, was diagnosed with hiv infection and was treated with RESCRIPTOR. After drug was administered, patient experienced the following problems/side effects: bone disorder, pathological fracture, . RESCRIPTOR dosage: unknown. During the same period patient was treated with ABACAVIR SULPHATE, LAMIVUDINE, FACTOR VIII. Patient was hospitalized and became disabled. Patient recovered.
Rescriptor Side Effects Report #5484601-8
RESCRIPTOR problem was reported by a Health Professional from CANADA on Oct 03, 2007. Male patient, weighting 208.1 lb, was diagnosed with hiv infection and was treated with RESCRIPTOR. After drug was administered, patient experienced the following problems/side effects: bone disorder, pathological fracture, . RESCRIPTOR dosage: unknown. During the same period patient was treated with ABACAVIR SULPHATE, LAMIVUDINE, FACTOR VIII. Patient was hospitalized and became disabled. Patient recovered.
Actos Side Effects Report #5501361-2
Physician from GERMANY reported ACTOS problem on Oct 19, 2007. Female patient, 50 years of age, was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: foot fracture, pathological fracture, . ACTOS dosage: unknown. Patient recovered.
Fosamax Side Effects Report #5453197-9
FOSAMAX problem was reported by a Physician from SINGAPORE on Sept 07, 2007. Female patient, 60 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: femur fracture, pathological fracture, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Viani Side Effects Report #5456562-9
Physician from GERMANY reported VIANI problem on Sept 12, 2007. Female patient, 50 years of age, was treated with VIANI. After drug was administered, patient experienced the following problems/side effects: oral fungal infection, pathological fracture, tooth fracture, . VIANI dosage: unknown. Patient recovered.
Fosamax Side Effects Report #5459797-4
FOSAMAX problem was reported by a Health Professional from JAPAN on Sept 07, 2007. Female patient, 78 years of age, weighting 85.98 lb, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: low turnover osteopathy, pathological fracture, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Viani Side Effects Report #5402718-0
Physician from GERMANY reported VIANI problem on July 27, 2007. Female patient, 50 years of age, was treated with VIANI. After drug was administered, patient experienced the following problems/side effects: jaw fracture, pathological fracture, . VIANI dosage: unknown. Patient recovered.
Bevacizumab Side Effects Report #5408820-1
BEVACIZUMAB problem was reported by a Physician from UNITED KINGDOM on July 26, 2007. Female patient was diagnosed with breast cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: humerus fracture, pathological fracture, . BEVACIZUMAB dosage: 880 MG, DAYS 1+15. During the same period patient was treated with CAELYX, NIFEDIPINE, METOPROLOL SUCCINATE, HYDROCHLOROTHIAZIDUM, ASPIRIN, PHENYTOIN, MORPHINE SULPHATE, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.
Viread Side Effects Report #5391633-7
Consumer or non-health professional from UNITED STATES reported VIREAD problem on July 05, 2007. Female patient, 45 years of age, was diagnosed with hiv infection and was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: fanconi syndrome, pathological fracture, . VIREAD dosage: unknown. During the same period patient was treated with LOPINAVIR, DIDANOSINE. Patient was hospitalized. Patient recovered.
Viread Side Effects Report #5394676-2
VIREAD problem was reported by a Consumer or non-health professional from UNITED STATES on July 05, 2007. Female patient, 45 years of age, was diagnosed with hiv infection and was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: fanconi syndrome acquired, pathological fracture, . VIREAD dosage: unknown. During the same period patient was treated with LOPINAVIR AND RITONAVIR, DIDANOSINE. Patient was hospitalized. Patient recovered.
Viread Side Effects Report #5391633-7
Consumer or non-health professional from UNITED STATES reported VIREAD problem on July 05, 2007. Female patient, 45 years of age, was diagnosed with hiv infection and was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: fanconi syndrome, pathological fracture, . VIREAD dosage: unknown. During the same period patient was treated with LOPINAVIR, DIDANOSINE. Patient was hospitalized. Patient recovered.
Viread Side Effects Report #5394676-2
VIREAD problem was reported by a Consumer or non-health professional from UNITED STATES on July 05, 2007. Female patient, 45 years of age, was diagnosed with hiv infection and was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: fanconi syndrome acquired, pathological fracture, . VIREAD dosage: unknown. During the same period patient was treated with LOPINAVIR AND RITONAVIR, DIDANOSINE. Patient was hospitalized. Patient recovered.
Revlimid Side Effects Report #5797639-8
Physician from UNITED STATES reported REVLIMID problem on June 25, 2008. Female patient, 84 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: cardio-respiratory arrest, pathological fracture, post procedural complication, . REVLIMID dosage: 5 MG, 1 IN 2 D, ORAL. Patient was hospitalized. Patient died on 02/25/2008.
Crixivan Side Effects Report #5737817-7
CRIXIVAN problem was reported by a Physician from SPAIN on May 07, 2008. Female patient, child 12 years of age, was diagnosed with hiv infection and was treated with CRIXIVAN. After drug was administered, patient experienced the following problems/side effects: no therapeutic response, pathological fracture, . CRIXIVAN dosage: unknown. During the same period patient was treated with LAMIVUDINE, ZIDOVUDINE. Patient recovered.
Crixivan Side Effects Report #5745365-3
Physician from SPAIN reported CRIXIVAN problem on May 07, 2008. Female patient, child 12 years of age, was diagnosed with hiv infection and was treated with CRIXIVAN. After drug was administered, patient experienced the following problems/side effects: no therapeutic response, pathological fracture, . CRIXIVAN dosage: unknown. During the same period patient was treated with LAMIVUDINE, ZIDOVUDINE. Patient recovered.
Atripla Side Effects Report #5694090-6
ATRIPLA problem was reported by a Physician from UNITED STATES on Mar 25, 2008. Male patient, 30 years of age, was treated with ATRIPLA. After drug was administered, patient experienced the following problems/side effects: osteonecrosis, pathological fracture, . ATRIPLA dosage: unknown. Patient recovered.
Topotecan Side Effects Report #5694405-9
Consumer or non-health professional from UNITED STATES reported TOPOTECAN problem on Apr 03, 2008. Female patient, weighting 149.7 lb, was treated with TOPOTECAN. After drug was administered, patient experienced the following problems/side effects: pain in extremity, pathological fracture, soft tissue disorder, spinal column stenosis, . TOPOTECAN dosage: 10.2 MG. During the same period patient was treated with LYRICA, PERCOCET. Patient was hospitalized. Patient recovered.