DEVICE RELATED INFECTION side effect
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Drugs associated with DEVICE RELATED INFECTION
ARANESP ARIXTRA AVASTIN AVONEX BEVACIZUMAB BEXTRA BIOCLEANSE CANCIDAS CARDIAC CELEBREX CEREZYME CETUXIMAB ENBREL EXJADE FABRAZYME FORTEO FOSAMAX HUMALOG HUMIRA INTRAUTERINE LIORESAL LISTERINE MORPHINE NATALIZUMAB ORENCIA OXALIPLATIN PEGINTERFERON PREMARIN PRIALT REBIF REMICADE TACROLIMUS TEMODAL TEMOZOLOMIDE TYSABRI VELCADE ZETIA ZOMETAEnbrel Side Effects Report #5662764-9
Consumer or non-health professional from SPAIN reported ENBREL problem on Feb 28, 2008. Female patient was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: device related infection, . ENBREL dosage: unknown. Patient recovered.
Fosamax Side Effects Report #5628578-0
FOSAMAX problem was reported by a Physician from UNITED STATES on Feb 05, 2008. Female patient, 74 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: device related infection, neck injury, osteomyelitis, subdural haematoma, uterine disorder, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Fabrazyme Side Effects Report #5637740-2
Pharmacist from UNITED STATES reported FABRAZYME problem on Feb 07, 2008. Male patient, 48 years of age, weighting 159.8 lb, was diagnosed with fabry's disease and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: device related infection, osteomyelitis, . FABRAZYME dosage: 70 MG, Q2W, INTRAVENOUS. Patient was hospitalized. Patient recovered.
Forteo Side Effects Report #5581281-8
FORTEO problem was reported by a Physician from UNITED STATES on Dec 20, 2007. Female patient was diagnosed with fracture and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: device related infection, fracture nonunion, osteomyelitis, streptococcal infection, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.
Forteo Side Effects Report #5584430-0
Consumer or non-health professional from SPAIN reported FORTEO problem on Dec 28, 2007. Female patient, 81 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: device related infection, joint injury, . FORTEO dosage: unknown. During the same period patient was treated with SEGURIL. Patient was hospitalized. Patient recovered.
Fosamax Side Effects Report #5601411-9
FOSAMAX problem was reported by a Physician from UNITED STATES on Jan 16, 2008. Female patient, 74 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: device related infection, neck injury, osteomyelitis, subdural haematoma, uterine disorder, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Exjade Side Effects Report #5604761-5
Health Professional from UNITED STATES reported EXJADE problem on Jan 25, 2008. Male patient, 55 years of age, weighting 295.0 lb, was diagnosed with iron metabolism disorder and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: device related infection, respiratory failure, sepsis, . EXJADE dosage: 2000 MG, QD. Patient died on 10/17/2007.
Lioresal Side Effects Report #5567657-3
LIORESAL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 05, 2007. Male patient was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: device related infection, eating disorder, haemorrhage intracranial, incision site erythema, intracranial aneurysm, meningitis, . LIORESAL dosage: unknown. Patient died on 12/03/2007.
Enbrel Side Effects Report #5523471-6
Physician from UNITED STATES reported ENBREL problem on Nov 12, 2007. Female patient, weighting 196.2 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: device related infection, knee arthroplasty, localised infection, rheumatoid arthritis, . ENBREL dosage: unknown. During the same period patient was treated with ARAVA. Patient was hospitalized. Patient recovered.
Lioresal Side Effects Report #5525404-5
LIORESAL problem was reported by a Physician from UNITED STATES on Jan 05, 2005. Male patient was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: device related infection, disease progression, scoliosis, staphylococcal infection, . LIORESAL dosage: unknown. Patient recovered.
Fosamax Side Effects Report #5528500-1
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Nov 27, 2007. Female patient, 74 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: device related infection, neck injury, osteomyelitis, subdural haematoma, uterine disorder, . FOSAMAX dosage: unknown. Patient was hospitalized. Patient recovered.
Natalizumab Side Effects Report #5531789-6
NATALIZUMAB problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 13, 2007. Male patient, 56 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: device related infection, hypotonia, nervous system disorder, . NATALIZUMAB dosage: 300 MG;QM;IV. Patient was hospitalized. Patient recovered.
Bevacizumab Side Effects Report #5485114-X
Consumer or non-health professional from UNITED STATES reported BEVACIZUMAB problem on Oct 09, 2007. Female patient was diagnosed with pancreatic carcinoma metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: device related infection, renal failure acute, . BEVACIZUMAB dosage: 10 MG. OVER 90MIN. IV. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5490642-7
HUMIRA problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Oct 09, 2007. Female patient, weighting 121.3 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: device related infection, joint arthroplasty, . HUMIRA dosage: unknown. During the same period patient was treated with LEFLUNOMIDE, AMITRIPTYLINE, INHALERS, MORPHINE SULPHATE, ACETAMINOPHEN W. Patient recovered.
Temozolomide Side Effects Report #5473200-X
Physician from UNITED KINGDOM reported TEMOZOLOMIDE problem on Sept 19, 2007. Male patient, 59 years of age, weighting 197.1 lb, was diagnosed with glioblastoma and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: device related infection, gastrointestinal disorder, . TEMOZOLOMIDE dosage: unknown. During the same period patient was treated with FELODIPINE, LEVOTHYROXINE, PHENYTOIN. Patient was hospitalized. Patient recovered.
Prialt Side Effects Report #5407964-8
PRIALT problem was reported by a Consumer or non-health professional from UNITED STATES on July 23, 2007. Female patient, 51 years of age, was diagnosed with arachnoiditis and was treated with PRIALT. After drug was administered, patient experienced the following problems/side effects: device related infection, hallucination, auditory, implant site reaction, insomnia, meningitis, oedema peripheral, pain, pneumonia, sepsis, . PRIALT dosage: unknown. During the same period patient was treated with DILAUDID. Patient was hospitalized. Patient recovered.
Humalog Side Effects Report #5427746-0
Consumer or non-health professional from UNITED STATES reported HUMALOG problem on Aug 20, 2007. Male patient, 74 years of age, was diagnosed with diabetes mellitus and was treated with HUMALOG. After drug was administered, patient experienced the following problems/side effects: device related infection, . HUMALOG dosage: unknown. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5392970-2
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on July 12, 2007. Female patient, 51 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: device related infection, post procedural complication, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Cancidas Side Effects Report #5397079-X
Physician from BRAZIL reported CANCIDAS problem on June 04, 2007. Female patient, 75 years of age, was diagnosed with device related infection, septic embolus and was treated with CANCIDAS. After drug was administered, patient experienced the following problems/side effects: device related infection, hepatitis, septic embolus, . CANCIDAS dosage: unknown. During the same period patient was treated with TARGOCID, POLYMYXIN B SULPHATE, HEPARIN, MAREVAN, PROPOFOL, FENTANYL, DORMONIDECTION. Patient died on 05/23/2007.
Celebrex Side Effects Report #5418822-7
CELEBREX problem was reported by a Consumer or non-health professional from UNITED STATES on July 12, 2006. Female patient was diagnosed with arthralgia and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: device related infection, migraine, osteoarthritis, staphylococcal infection, . CELEBREX dosage: 200 MG (200 MG, 1 IN 1 D). During the same period patient was treated with ARICEPT, WARFARIN. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5392970-2
Consumer or non-health professional from UNITED STATES reported AVONEX problem on July 12, 2007. Female patient, 51 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: device related infection, post procedural complication, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Cancidas Side Effects Report #5397079-X
CANCIDAS problem was reported by a Physician from BRAZIL on June 04, 2007. Female patient, 75 years of age, was diagnosed with device related infection, septic embolus and was treated with CANCIDAS. After drug was administered, patient experienced the following problems/side effects: device related infection, hepatitis, septic embolus, . CANCIDAS dosage: unknown. During the same period patient was treated with TARGOCID, POLYMYXIN B SULPHATE, HEPARIN, MAREVAN, PROPOFOL, FENTANYL, DORMONIDECTION. Patient died on 05/23/2007.
Celebrex Side Effects Report #5418822-7
Consumer or non-health professional from UNITED STATES reported CELEBREX problem on July 12, 2006. Female patient was diagnosed with arthralgia and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: device related infection, migraine, osteoarthritis, staphylococcal infection, . CELEBREX dosage: 200 MG (200 MG, 1 IN 1 D). During the same period patient was treated with ARICEPT, WARFARIN. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5763022-4
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on May 20, 2008. Male patient, 54 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: device related infection, pneumonia aspiration, staphylococcal infection, thrombosis, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Biocleanse Side Effects Report #5773097-4
Health Professional from UNITED STATES reported BIOCLEANSE TIBIALIS POSTERIOR TENDON problem on Apr 03, 2008. Male patient, 29 years of age, was treated with BIOCLEANSE TIBIALIS POSTERIOR TENDON. After drug was administered, patient experienced the following problems/side effects: device related infection, erythema, induration, pain, swelling, . BIOCLEANSE TIBIALIS POSTERIOR TENDON dosage: unknown. Patient recovered.
Zetia Side Effects Report #5731924-0
ZETIA problem was reported by a Health Professional from UNITED KINGDOM on May 01, 2008. Male patient, 69 years of age, was treated with ZETIA. After drug was administered, patient experienced the following problems/side effects: device related infection, pneumonia, rhabdomyolysis, . ZETIA dosage: unknown. During the same period patient was treated with ATORVASTATIN, FUSIDATE. Patient was hospitalized. Patient recovered.
Zetia Side Effects Report #5735028-2
Health Professional from UNITED KINGDOM reported ZETIA problem on May 01, 2008. Male patient, 69 years of age, was treated with ZETIA. After drug was administered, patient experienced the following problems/side effects: device related infection, pneumonia, rhabdomyolysis, . ZETIA dosage: unknown. During the same period patient was treated with ATORVASTATIN, FUSIDATE. Patient was hospitalized. Patient recovered.
Biocleanse Side Effects Report #5748482-7
BIOCLEANSE TIBIALIS POSTERIOR TENDON problem was reported by a Health Professional from UNITED STATES on Apr 03, 2008. Male patient, 29 years of age, was treated with BIOCLEANSE TIBIALIS POSTERIOR TENDON. After drug was administered, patient experienced the following problems/side effects: device related infection, . BIOCLEANSE TIBIALIS POSTERIOR TENDON dosage: unknown. Patient recovered.
Bevacizumab Side Effects Report #5713406-5
Health Professional from UNITED STATES reported BEVACIZUMAB problem on Apr 09, 2008. Female patient, weighting 220.0 lb, was diagnosed with tonsil cancer, pain and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: device related infection, oesophagitis, vomiting, . BEVACIZUMAB dosage: 15 MG/KG, UNK. During the same period patient was treated with ERLOTINIB, PACLITAXEL, RADIATION, DILAUDID. Patient was hospitalized. Patient recovered.
Orencia Side Effects Report #5713940-8
ORENCIA problem was reported by a Physician from UNITED STATES on Apr 22, 2008. Male patient, 44 years of age, was diagnosed with rheumatoid arthritis and was treated with ORENCIA. After drug was administered, patient experienced the following problems/side effects: device related infection, staphylococcal infection, . ORENCIA dosage: 750MG EVERY 4 WEEKS I.V.. Patient was hospitalized and became disabled. Patient recovered.
Cardiac Side Effects Report #5361473-3
Health Professional from UNITED STATES reported CARDIAC problem on June 15, 2007. Female patient, 63 years of age, weighting 110.2 lb, was diagnosed with aortic stenosis and was treated with CARDIAC. After drug was administered, patient experienced the following problems/side effects: device related infection, surgical procedure repeated, . CARDIAC dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.
Arixtra Side Effects Report #5304446-9
ARIXTRA problem was reported by a Pharmacist from UNITED STATES on Apr 17, 2007. Male patient was diagnosed with deep vein thrombosis, disease recurrence and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: device related infection, haematoma, medical device site reaction, pacemaker complication, . ARIXTRA dosage: 7.5 MG QD SQ. During the same period patient was treated with WARFARIN. Patient was hospitalized. Patient recovered.
Morphine Side Effects Report #5268231-9
Health Professional from UNITED STATES reported MORPHINE SULPHATE problem on Mar 02, 2007. Male patient, 47 years of age, was treated with MORPHINE SULPHATE. After drug was administered, patient experienced the following problems/side effects: device related infection, diplegia, infusion site abscess, infusion site mass, spinal cord compression, streptococcal infection, . MORPHINE SULPHATE dosage: 32 MG, 1 IN D, INTRATHECAL. Patient recovered.
Enbrel Side Effects Report #5275605-9
ENBREL problem was reported by a Consumer or non-health professional from GERMANY on Mar 13, 2007. Female patient, 75 years of age, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: device related infection, salmonella sepsis, . ENBREL dosage: unknown. During the same period patient was treated with LANTAREL. Patient was hospitalized. Patient recovered.
Temodal Side Effects Report #5278068-2
Physician from FRANCE reported TEMODAL problem on Mar 15, 2007. Female patient, child 10 years of age, was diagnosed with malignant glioma and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: device related infection, febrile bone marrow aplasia, haemoglobin decreased, platelet count decreased, staphylococcal sepsis, . TEMODAL dosage: 200 MG; QD; PO. During the same period patient was treated with CISPLATIN. Patient was hospitalized. Patient recovered.
Premarin Side Effects Report #5678196-3
PREMARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 13, 2008. Female patient, weighting 157.1 lb, was treated with PREMARIN. After drug was administered, patient experienced the following problems/side effects: breast cancer metastatic, device related infection, metastases to lymph nodes, oestrogen receptor assay positive, progesterone receptor assay positive, . PREMARIN dosage: unknown. During the same period patient was treated with ESTRATEST, PROVERA. Patient recovered.
Humira Side Effects Report #5620494-3
Physician from GERMANY reported HUMIRA problem on Jan 29, 2008. Female patient, 66 years of age, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthralgia, device related infection, empyema, ischaemic cerebral infarction, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISOLONE, BISOPROLOL FUMARATE, BISOPROLOL FUMARATE, METFORMIN, ALENDRON, LEKOVIT CA, METHOTREXATE, SIMVASTATIN. Patient was hospitalized. Patient recovered.
Forteo Side Effects Report #5631949-X
FORTEO problem was reported by a Physician from ITALY on Feb 11, 2008. Male patient was diagnosed with lower limb fracture and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, device related infection, dysuria, jaundice, lymphadenopathy, lymphoma, oedema peripheral, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5534685-3
Consumer or non-health professional from UNITED KINGDOM reported HUMIRA problem on Nov 27, 2007. Female patient, weighting 134.5 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: clostridial infection, device related infection, diarrhoea, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, DICLOFENAC, FOLIC ACID, HYDROXYCHLOROQUINE SULPHATE, SULFASALAZINE. Patient was hospitalized. Patient recovered.
Enbrel Side Effects Report #5536884-3
ENBREL problem was reported by a Physician from UNITED STATES on Feb 15, 2007. Female patient, weighting 133.2 lb, was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: cough, device related infection, staphylococcal infection, . ENBREL dosage: unknown. During the same period patient was treated with CARDIZEM, DIGOXIN, PREMARIN, RANITIDINE, LIPITOR, ASPIRIN, VITAMIN CAP, TYLENOL. Patient was hospitalized. Patient recovered.
Oxaliplatin Side Effects Report #5541741-2
Health Professional from UNITED STATES reported OXALIPLATIN problem on Dec 05, 2007. Male patient, 49 years of age, was diagnosed with lung neoplasm malignant and was treated with OXALIPLATIN. After drug was administered, patient experienced the following problems/side effects: cellulitis, device related infection, erythema, oedema peripheral, pain, . OXALIPLATIN dosage: 85MG/M2 DAY 1-15 Q28DAYS IV. Patient was hospitalized. Patient recovered.
Listerine Side Effects Report #5553070-1
LISTERINE WHITENING PRE problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 29, 2007. Male patient was diagnosed with dental disorder prophylaxis and was treated with LISTERINE WHITENING PRE. After drug was administered, patient experienced the following problems/side effects: bacterial infection, device related infection, oral mucosal exfoliation, . LISTERINE WHITENING PRE dosage: unknown. Patient recovered.
Lioresal Side Effects Report #5568154-1
Physician from UNITED STATES reported LIORESAL problem on Dec 03, 2007. Male patient was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: convulsion, device related infection, intracranial hypotension, staphylococcal infection, surgical procedure repeated, . LIORESAL dosage: unknown. Patient was hospitalized. Patient recovered.
Enbrel Side Effects Report #5486637-X
ENBREL problem was reported by a Health Professional from UNITED KINGDOM on Oct 04, 2007. Female patient, 58 years of age, weighting 189.6 lb, was diagnosed with rheumatoid arthritis, dyspepsia and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: arthritis bacterial, device related infection, joint arthroplasty, staphylococcal infection, . ENBREL dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, PROPYLENE GLYCOL, HYDROXYCHLOROQUINE SULPHATE, NAPROXEN, PREDNISOLONE, OMEPRAZOLE. Patient was hospitalized. Patient recovered.
Zometa Side Effects Report #5492729-1
Consumer or non-health professional from UNITED STATES reported ZOMETA problem on Oct 16, 2007. Female patient, 65 years of age, weighting 142.0 lb, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: computerised tomogram abnormal, device related infection, face and mouth x-ray abnormal, failure of implant, gingival oedema, gingival recession, impaired healing, loose tooth, . ZOMETA dosage: 4 MG, UNK. During the same period patient was treated with ARIMIDEX, FASLODEX, COUMADIN, EFFEXOR, AREDIA. Patient recovered.
Humira Side Effects Report #5472078-8
HUMIRA problem was reported by a Physician from GERMANY on Sept 20, 2007. Female patient, 66 years of age, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthralgia, device related infection, empyema, ischaemic cerebral infarction, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISOLONE, BISOPROLOL FUMARATE, BISOPROLOL FUMARATE, METFORMIN, ALENDRON, LEKOVIT CA, METHOTREXATE, SIMVASTATIN. Patient was hospitalized. Patient recovered.
Rebif Side Effects Report #5416410-X
Consumer or non-health professional from UNITED STATES reported REBIF problem on Aug 02, 2007. Female patient, 51 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: depression, device related infection, meningitis bacterial, staphylococcal infection, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.
Cerezyme Side Effects Report #5378500-X
CEREZYME problem was reported by a Physician from JAPAN on June 21, 2007. Female patient, child 8 years of age, weighting 26.46 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase increased, device related infection, enterocolitis, heat stroke, hepatocellular damage, muscle injury, pneumonia, upper respiratory tract inflammation, urinary tract infection, . CEREZYME dosage: unknown. During the same period patient was treated with VALPROATE, CLONAZEPAM, FAMOTIDINE, DOMPERIDONE, DIAZEPAM, DANTROLENE, ZONISAMIDE, FUROSEMIDE. Patient was hospitalized. Patient recovered.
Cerezyme Side Effects Report #5378500-X
Physician from JAPAN reported CEREZYME problem on June 21, 2007. Female patient, child 8 years of age, weighting 26.46 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase increased, device related infection, enterocolitis, heat stroke, hepatocellular damage, muscle injury, pneumonia, upper respiratory tract inflammation, urinary tract infection, . CEREZYME dosage: unknown. During the same period patient was treated with VALPROATE, CLONAZEPAM, FAMOTIDINE, DOMPERIDONE, DIAZEPAM, DANTROLENE, ZONISAMIDE, FUROSEMIDE. Patient was hospitalized. Patient recovered.
Aranesp Side Effects Report #5728559-2
ARANESP problem was reported by a Physician from NETHERLANDS on Apr 25, 2008. Male patient, weighting 188.5 lb, was diagnosed with myelodysplastic syndrome and was treated with ARANESP. After drug was administered, patient experienced the following problems/side effects: atrioventricular block complete, device related infection, . ARANESP dosage: unknown. During the same period patient was treated with ASCAL, OMNIC, FOLIC ACID. Patient was hospitalized and became disabled. Patient recovered.
Bextra Side Effects Report #5733710-4
Consumer or non-health professional from UNITED STATES reported BEXTRA problem on Apr 28, 2008. Female patient, weighting 299.8 lb, was diagnosed with arthritis and was treated with BEXTRA. After drug was administered, patient experienced the following problems/side effects: coronary artery occlusion, device related infection, diabetes mellitus, impaired healing, myocardial infarction, post procedural complication, thyroid disorder, wound complication, wound secretion, . BEXTRA dosage: unknown. Patient was hospitalized. Patient recovered.