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ANAEMIA OF CHRONIC DISEASE side effect

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Fosamax Side Effects Report #5655369-7
Physician from UNITED STATES reported FOSAMAX problem on Feb 27, 2008. Female patient, 64 years of age, was diagnosed with osteoporosis, thyroid disorder and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, anxiety, bronchitis, central line infection, depression, encephalopathy, enterococcal infection, musculoskeletal discomfort, osteomyelitis, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5657147-1
FOSAMAX problem was reported by a Health Professional from UNITED STATES on Feb 26, 2008. Female patient, weighting 134.5 lb, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, arthralgia, breast disorder, cellulitis, circulatory collapse, depression, fatigue, gastrooesophageal reflux disease, herpes zoster ophthalmic, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5688682-8
Physician from UNITED STATES reported FOSAMAX problem on Mar 21, 2008. Female patient, 87 years of age, weighting 143.3 lb, was diagnosed with osteoporosis, osteoarthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, anxiety, arthralgia, cardiac failure congestive, cerebral ischaemia, compression fracture, constipation, contusion, fall, . FOSAMAX dosage: unknown. During the same period patient was treated with CELEBREX. Patient was hospitalized. Patient died on 05/31/2006.

Fosamax Side Effects Report #5612390-2
FOSAMAX problem was reported by a Physician from UNITED STATES on Jan 24, 2008. Female patient, 87 years of age, weighting 143.3 lb, was diagnosed with osteoporosis, osteoarthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, anxiety, arthralgia, cardiac failure congestive, cerebral ischaemia, compression fracture, constipation, contusion, fall, . FOSAMAX dosage: unknown. During the same period patient was treated with CELEBREX. Patient was hospitalized. Patient died on 05/31/2006.


Enbrel Side Effects Report #5629582-9
Physician from UNITED STATES reported ENBREL problem on Feb 07, 2008. Female patient, weighting 130.1 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, ankle fracture, fall, femur fracture, hepatic cirrhosis, hypothyroidism, osteoporosis, raynaud's phenomenon, rheumatoid arthritis, . ENBREL dosage: unknown. During the same period patient was treated with SYNTHROID, PLAQUENIL, COLACE, ROXICODONE, VITAMIN CAP, MAGNESIUM, NEXIUM, ALDACTONE. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5629731-2
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 07, 2008. Female patient, 64 years of age, was diagnosed with osteoporosis, thyroid disorder and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, anxiety, bronchitis, central line infection, depression, encephalopathy, enterococcal infection, musculoskeletal discomfort, osteomyelitis, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Aredia Side Effects Report #5635970-7
Consumer or non-health professional from UNITED STATES reported AREDIA problem on Feb 12, 2008. Female patient, 70 years of age, weighting 180.0 lb, was diagnosed with multiple myeloma, anxiety and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, anaphylactic reaction, angioedema, biopsy, biopsy lung, bone disorder, bone neoplasm malignant, bronchiectasis, decreased appetite, . AREDIA dosage: 90 MG OVER 4 HOURS. During the same period patient was treated with PREDNISONE, ATIVAN, EFFEXOR, PREMPHASE, NEURONTIN, ZOFRAN. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5509374-1
FOSAMAX problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 02, 2007. Female patient, 87 years of age, weighting 143.3 lb, was diagnosed with osteoporosis, osteoarthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, anxiety, arthralgia, cardiac failure congestive, compression fracture, contusion, fall, fatigue, gastroenteritis viral, . FOSAMAX dosage: unknown. During the same period patient was treated with CELEBREX. Patient was hospitalized. Patient died on 05/31/2006.

Fosamax Side Effects Report #5518815-5
Physician from UNITED STATES reported FOSAMAX problem on Nov 07, 2007. Female patient, 87 years of age, weighting 143.3 lb, was diagnosed with osteoporosis, osteoarthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, anxiety, arthralgia, cardiac failure congestive, compression fracture, contusion, fall, fatigue, gastroenteritis viral, . FOSAMAX dosage: unknown. During the same period patient was treated with CELEBREX. Patient was hospitalized. Patient died on 05/31/2006.


Fosamax Side Effects Report #5521016-8
FOSAMAX problem was reported by a Physician from UNITED STATES on Nov 14, 2007. Female patient, 87 years of age, weighting 143.3 lb, was diagnosed with osteoporosis, osteoarthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, anxiety, arthralgia, cardiac failure congestive, compression fracture, contusion, fall, fatigue, gastroenteritis viral, . FOSAMAX dosage: unknown. During the same period patient was treated with CELEBREX. Patient was hospitalized. Patient died on 05/31/2006.

Fosamax Side Effects Report #5527986-6
Physician from UNITED STATES reported FOSAMAX problem on Nov 19, 2007. Female patient, 87 years of age, weighting 143.3 lb, was diagnosed with osteoporosis, osteoarthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, anxiety, arthralgia, cardiac failure congestive, compression fracture, contusion, fall, fatigue, gastroenteritis viral, . FOSAMAX dosage: unknown. During the same period patient was treated with CELEBREX. Patient was hospitalized. Patient died on 05/31/2006.

Enbrel Side Effects Report #5486627-7
ENBREL problem was reported by a Physician from UNITED STATES on Oct 04, 2007. Female patient, weighting 130.1 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, ankle fracture, fall, femur fracture, hepatic cirrhosis, hypothyroidism, osteoporosis, raynaud's phenomenon, rheumatoid arthritis, . ENBREL dosage: unknown. During the same period patient was treated with SYNTHROID, PLAQUENIL, COLACE, ROXICODONE, VITAMIN CAP, MAGNESIUM SULPHATE, NEXIUM, ALDACTONE. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5495323-1
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Oct 15, 2007. Female patient, 87 years of age, weighting 143.3 lb, was diagnosed with osteoporosis, osteoarthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, anxiety, arthralgia, cardiac failure congestive, compression fracture, contusion, dental fistula, depression, dyspnoea, . FOSAMAX dosage: unknown. During the same period patient was treated with CELEBREX. Patient was hospitalized. Patient died on 05/31/2006.

Cisplatin Side Effects Report #5449907-7
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 10, 2007. Female patient, weighting 145.0 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, dehydration, ejection fraction decreased, fluid retention, hydronephrosis, pericardial effusion, platelet count decreased, pulmonary oedema, renal failure acute, . CISPLATIN dosage: 88 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, TAXOL. Patient was hospitalized. Patient recovered.


Fosamax Side Effects Report #5453192-X
Physician from UNITED STATES reported FOSAMAX problem on Sept 05, 2007. Female patient, 72 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, colitis ischaemic, depression, diarrhoea, fall, gastroenteritis, glaucoma, hip fracture, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5466181-6
FOSAMAX problem was reported by a Physician from UNITED STATES on Sept 19, 2007. Female patient, 72 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, colitis ischaemic, depression, diarrhoea, fall, gastroenteritis, glaucoma, hip fracture, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5423770-2
Physician from UNITED STATES reported FOSAMAX problem on Aug 16, 2007. Female patient, 72 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, colitis ischaemic, depression, diarrhoea, fall, gastroenteritis, glaucoma, hip fracture, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Myozyme Side Effects Report #5442145-3
MYOZYME problem was reported by a Physician from UNITED STATES on Aug 15, 2007. Male patient, 22 years of age, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, arthralgia, arthritis, hypochromic anaemia, lymphadenopathy, oedema peripheral, pain in extremity, pain in jaw, platelet count increased, . MYOZYME dosage: 20 MG/KG Q2WKS IV. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5381935-2
Physician from UNITED STATES reported FOSAMAX problem on June 26, 2007. Female patient, 72 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, colitis ischaemic, depression, diarrhoea, fall, gastroenteritis, glaucoma, hip fracture, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.


Betaseron Side Effects Report #5395575-2
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on July 13, 2007. Male patient, 67 years of age, weighting 160.0 lb, was diagnosed with secondary progressive multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, cardiac failure congestive, cardiomyopathy, intracardiac thrombus, mitral valve disease, myocardial infarction, myocardial ischaemia, pleural effusion, urinary tract infection, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Cellcept Side Effects Report #5403772-2
Physician from UNITED STATES reported CELLCEPT problem on May 26, 2005. Female patient, 54 years of age, weighting 159.4 lb, was diagnosed with prophylaxis, prophylaxis against transplant rejection, renal transplant, nephrogenic anaemia and was treated with CELLCEPT. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, diverticulitis, platelet count decreased, therapeutic response decreased, white blood cell count decreased, . CELLCEPT dosage: unknown. During the same period patient was treated with PROCRIT, EPOGEN, NEORAL, PREDNISONE, LOPRESSOR. Patient recovered.

Fosamax Side Effects Report #5381935-2
FOSAMAX problem was reported by a Physician from UNITED STATES on June 26, 2007. Female patient, 72 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, colitis ischaemic, depression, diarrhoea, fall, gastroenteritis, glaucoma, hip fracture, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5395575-2
Consumer or non-health professional from UNITED STATES reported BETASERON problem on July 13, 2007. Male patient, 67 years of age, weighting 160.0 lb, was diagnosed with secondary progressive multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, cardiac failure congestive, cardiomyopathy, intracardiac thrombus, mitral valve disease, myocardial infarction, myocardial ischaemia, pleural effusion, urinary tract infection, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Cellcept Side Effects Report #5403772-2
CELLCEPT problem was reported by a Physician from UNITED STATES on May 26, 2005. Female patient, 54 years of age, weighting 159.4 lb, was diagnosed with prophylaxis, prophylaxis against transplant rejection, renal transplant, nephrogenic anaemia and was treated with CELLCEPT. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, diverticulitis, platelet count decreased, therapeutic response decreased, white blood cell count decreased, . CELLCEPT dosage: unknown. During the same period patient was treated with PROCRIT, EPOGEN, NEORAL, PREDNISONE, LOPRESSOR. Patient recovered.

Mevacor Side Effects Report #5760238-8
Health Professional from UNITED STATES reported MEVACOR problem on May 19, 2008. Female patient, 71 years of age, weighting 115.0 lb, was diagnosed with osteoporosis and was treated with MEVACOR. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, aortic valve replacement, bladder neoplasm, cerebral infarction, coronary artery disease, disease recurrence, myocardial infarction, osteoarthritis, pancreatic neoplasm, . MEVACOR dosage: 80 MG/DAILY/PO. During the same period patient was treated with LASOFOXIFENE UNK, COZAAR, ALENDRONATE, AMOXICILLIN, CYANOCOBALAMIN, FERROUS SULPHATE, INSULIN. Patient was hospitalized. Patient died on 09/26/2007.

Enbrel Side Effects Report #5788683-5
ENBREL problem was reported by a Physician from UNITED STATES on June 17, 2008. Female patient, weighting 149.0 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, back pain, blood potassium decreased, bronchitis, bursitis, colonic polyp, gait disturbance, labile blood pressure, memory impairment, . ENBREL dosage: unknown. During the same period patient was treated with TRICOR, AMITIZA, LAXATIVES, TYLENOL, ASCORBIC ACID, DARVOCET, DOXYCYCLINE HYCLATE, LORAZEPAM. Patient was hospitalized and became disabled. Patient recovered.

Gemzar Side Effects Report #5708076-6
Physician from UNITED STATES reported GEMZAR problem on Apr 07, 2008. Male patient, weighting 166.0 lb, was diagnosed with non-small cell lung cancer stage i, cellulitis, back pain and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, blood potassium decreased, cellulitis, diarrhoea, dizziness, dyspepsia, dysphagia, dyspnoea, fatigue, . GEMZAR dosage: unknown. During the same period patient was treated with KEFLEX, CISPLATIN, FLOMAX, NICORETTE, HYDREA, VITAMIN B, OXYCODONE. Patient was hospitalized. Patient recovered.

Keflex Side Effects Report #5715492-5
KEFLEX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 07, 2008. Male patient, 69 years of age, weighting 166.0 lb, was diagnosed with cellulitis, non-small cell lung cancer and was treated with KEFLEX. After drug was administered, patient experienced the following problems/side effects: anaemia of chronic disease, blood bicarbonate increased, blood glucose increased, blood potassium decreased, catheter related complication, cellulitis, diarrhoea, dizziness, dyspepsia, . KEFLEX dosage: unknown. During the same period patient was treated with GEMZAR, CISPLATIN, VITAMIN CAP, FLOMAX, NICORETTE, HYDREA, VITAMIN B12, OXYCODONE. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5665131-7
Physician from UNITED STATES reported FOSAMAX problem on Mar 05, 2008. Female patient, 64 years of age, was diagnosed with osteoporosis, thyroid disorder and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal injury, anaemia of chronic disease, anxiety, bradycardia, bronchitis, cardiac failure congestive, central line infection, dehydration, depression, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5677307-3
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 14, 2008. Female patient, 64 years of age, was diagnosed with osteoporosis, thyroid disorder and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal injury, anaemia of chronic disease, anxiety, bradycardia, bronchitis, cardiac failure congestive, central line infection, dehydration, depression, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5684459-8
Physician from UNITED STATES reported FOSAMAX problem on Mar 19, 2008. Female patient, 64 years of age, was diagnosed with osteoporosis, thyroid disorder and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal injury, anaemia of chronic disease, anxiety, bradycardia, bronchitis, cardiac failure congestive, central line infection, dehydration, depression, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5638832-4
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 15, 2008. Female patient, 72 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, anaemia of chronic disease, bronchitis, bursitis, cardiac failure congestive, chronic obstructive pulmonary disease, colitis ischaemic, compression fracture, deafness, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Aredia Side Effects Report #5605844-6
Consumer or non-health professional from UNITED STATES reported AREDIA problem on Jan 21, 2008. Female patient, 64 years of age, weighting 165.0 lb, was diagnosed with resorption bone increased and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: alveoloplasty, anaemia of chronic disease, anxiety, arteriovenous shunt operation, biopsy, blood creatinine increased, bone disorder, cataract, cataract operation, . AREDIA dosage: 90 MG MONTHLY. During the same period patient was treated with ZOMETA, NORVASC, MAXZIDE, DECADRON, CALCITRIOL, LISINOPRIL, PENICILLIN, VITAMIN B6. Patient recovered.

Fosamax Side Effects Report #5564212-6
FOSAMAX problem was reported by a Physician from UNITED STATES on Dec 12, 2007. Female patient, 50 years of age, was diagnosed with osteoporosis, osteopenia, pain and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: afferent loop syndrome, anaemia of chronic disease, anxiety, depression, dysphagia, lower limb fracture, obstruction gastric, oral infection, osteonecrosis, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Aredia Side Effects Report #5521685-2
Consumer or non-health professional from UNITED STATES reported AREDIA problem on Nov 12, 2007. Female patient, 64 years of age, weighting 207.0 lb, was diagnosed with resorption bone increased and was treated with AREDIA. After drug was administered, patient experienced the following problems/side effects: alveoloplasty, anaemia of chronic disease, anxiety, arteriovenous shunt operation, biopsy, blood creatinine increased, bone disorder, dialysis, injury, . AREDIA dosage: 90 MG MONTHLY. During the same period patient was treated with ZOMETA, NORVASC, MAXZIDE. Patient recovered.

Actonel Side Effects Report #5556752-0
ACTONEL problem was reported by a Physician from UNITED STATES on Aug 15, 2007. Female patient was diagnosed with osteopenia and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: abscess oral, anaemia of chronic disease, cellulitis, contusion, dental fistula, facial pain, hypoaesthesia, jaw disorder, osteomyelitis, . ACTONEL dosage: 35 MG, ONCE WEEKLY. During the same period patient was treated with MELOXICAM, ATENOLOL, HYDROCORTISONE, WELLBUTRIN, ESTRADIOL, ACIPHEX, MOBIC, COZAAR. Patient recovered.

Fosamax Side Effects Report #5501269-2
Physician from UNITED STATES reported FOSAMAX problem on Oct 23, 2007. Female patient, 50 years of age, was diagnosed with osteoporosis, pain and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: afferent loop syndrome, anaemia of chronic disease, anxiety, bone disorder, cheilitis, dental caries, depression, dysphagia, edentulous, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5470232-2
FOSAMAX problem was reported by a Physician from UNITED STATES on Sept 24, 2007. Female patient, 72 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, anaemia of chronic disease, cardiac failure congestive, colitis ischaemic, compression fracture, depression, diarrhoea, fall, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5430321-5
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Aug 21, 2007. Female patient was diagnosed with prophylaxis, osteopenia, gynaecomastia and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: amnesia, anaemia of chronic disease, anhedonia, anxiety, bone debridement, disability, erectile dysfunction, hot flush, hypercholesterolaemia, . ZOMETA dosage: 4 MG EVERY MONTH. During the same period patient was treated with FOSAMAX, TAMOXIFEN CITRATE, TRAZODONE, NIZORAL, AVODART, LUPRON, HYDROCORTISONE, CELEBREX. Patient recovered.

Fosamax Side Effects Report #5735056-7
FOSAMAX problem was reported by a Health Professional from UNITED STATES on May 07, 2008. Female patient, 60 years of age, weighting 134.5 lb, was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal pain lower, anaemia of chronic disease, arthralgia, breast disorder, cellulitis, circulatory collapse, depression, fatigue, gastrooesophageal reflux disease, . FOSAMAX dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Boniva Side Effects Report #5708261-3
Consumer or non-health professional from UNITED STATES reported BONIVA problem on Apr 08, 2008. Female patient, 78 years of age, was diagnosed with osteopenia, hypertension and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: anaemia, anaemia of chronic disease, anorexia, chondrocalcinosis pyrophosphate, mobility decreased, nausea, polymyalgia rheumatica, synovial cyst, vomiting, . BONIVA dosage: OTHER INDICATION: HYPERPARATHYROID, STRENGTH: 3MG/3ML. During the same period patient was treated with CALCIUM, GLUCOSAMINE, VITAMIN. Patient was hospitalized. Patient recovered.

Lotrel Side Effects Report #5336911-2
LOTREL problem was reported by a Physician from UNITED STATES on May 15, 2007. Male patient, 84 years of age, weighting 165.4 lb, was diagnosed with hypertension, benign prostatic hyperplasia, urinary incontinence and was treated with LOTREL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, anaemia of chronic disease, anuria, dysphagia, fall, head injury, lumbar spinal stenosis, muscular weakness, . LOTREL dosage: unknown. During the same period patient was treated with FLOMAX, DETROL, LIPITOR, CALCIUM CARBONATE W, ALLOPURINOL. Patient was hospitalized. Patient recovered.

Lotrel Side Effects Report #5339517-4
Physician from UNITED STATES reported LOTREL problem on May 15, 2007. Male patient, 84 years of age, weighting 165.4 lb, was diagnosed with hypertension, benign prostatic hyperplasia, urinary incontinence and was treated with LOTREL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, anaemia of chronic disease, anuria, dysphagia, fall, head injury, lumbar spinal stenosis, muscular weakness, . LOTREL dosage: unknown. During the same period patient was treated with FLOMAX, DETROL, LIPITOR, CALCIUM CARBONATE W, ALLOPURINOL. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5510866-X
VELCADE problem was reported by a Physician from UNITED STATES on Oct 29, 2007. Male patient, 66 years of age, weighting 226.0 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, alveolitis allergic, anaemia of chronic disease, cardiac failure congestive, diarrhoea, eosinophilic pneumonia, lung injury, . VELCADE dosage: 1.00 MG/M2, INTRAVENOUS. During the same period patient was treated with DEXAMETHASONE, DOXIL, ZOLOFT, FAMOTIDINE, ATROVENT HFA, PROCRIT. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5517831-7
Physician from UNITED STATES reported VELCADE problem on Nov 02, 2007. Male patient, 66 years of age, weighting 226.0 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, alveolitis allergic, anaemia of chronic disease, cardiac failure congestive, diarrhoea, interstitial lung disease, pulmonary eosinophilia, . VELCADE dosage: 1.00 MG/M2, INTRAVENOUS. During the same period patient was treated with DEXAMETHASONE, DOXIL, ZOLOFT, FAMOTIDINE, ATROVENT HFA, PROCRIT. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5500709-2
VELCADE problem was reported by a Physician from UNITED STATES on Oct 16, 2007. Male patient, 66 years of age, weighting 226.0 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, alveolitis allergic, anaemia of chronic disease, cardiac failure congestive, diarrhoea, fatigue, interstitial lung disease, . VELCADE dosage: 1.00 MG/M2, INTRAVENOUS. During the same period patient was treated with DEXAMETHASONE, DOXIL, ZOLOFT, FAMOTIDINE, ATROVENT HFA, PROCRIT. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5767401-0
Health Professional from UNITED STATES reported FOSAMAX problem on June 06, 2008. Female patient, 59 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia, anaemia of chronic disease, arteriosclerosis coronary artery, asthenia, azotaemia, back pain, bone disorder, bone neoplasm, . FOSAMAX dosage: unknown. During the same period patient was treated with ZOMETA. Patient was hospitalized and became disabled. Patient died.

Zofran Side Effects Report #5262189-4
ZOFRAN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 05, 2007. Female patient, 62 years of age, weighting 200.0 lb, was diagnosed with prophylaxis and was treated with ZOFRAN. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, abscess, anaemia of chronic disease, ascites, asthenia, blood creatinine increased, blood urea increased, bone operation, cardiac murmur, . ZOFRAN dosage: unknown. During the same period patient was treated with AREDIA, ZOMETA, PRINIVIL, COUMADIN, METOPROLOL SUCCINATE, PREVACID, LORAZEPAM. Patient was hospitalized. Patient died.

Velcade Side Effects Report #5268411-2
Physician from UNITED STATES reported VELCADE problem on Mar 02, 2007. Male patient, 66 years of age, weighting 226.0 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, alveolitis allergic, anaemia of chronic disease, cardiac failure acute, cardiac failure congestive, diarrhoea, eosinophilic pneumonia, pulmonary hypertension, . VELCADE dosage: unknown. During the same period patient was treated with DEXAMETHASONE, DOXIL, ZOLOFT, FAMOTIDINE, ATROVENT HFA, PROCRIT. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5282597-5
VELCADE problem was reported by a Physician from UNITED STATES on Mar 15, 2007. Male patient, 66 years of age, weighting 226.0 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, alveolitis allergic, anaemia of chronic disease, cardiac failure congestive, condition aggravated, diarrhoea, eosinophilic pneumonia, fatigue, . VELCADE dosage: 1.00 MG/M2, INTRAVENOUS. During the same period patient was treated with DEXAMETHASONE, DOXIL, ZOLOFT, FAMOTIDINE, ATROVENT HFA, PROCRIT. Patient was hospitalized. Patient recovered.