DEVICE RELATED INFECTION side effect
What is DEVICE RELATED INFECTION ?Drugs associated with DEVICE RELATED INFECTION
AVONEX BEVACIZUMAB CANCIDAS CELEBREX CELECOXIB CEREZYME CETUXIMAB ENBREL EXJADE FABRAZYME FORTEO FOSAMAX HEPARIN HUMALOG HUMIRA LIORESAL LISTERINE NATALIZUMAB OXALIPLATIN PEGINTERFERON PREMARIN PRIALT REBIF TEMOZOLOMIDE VELCADE ZOMETADEVICE RELATED INFECTION : Enbrel 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : Heparin Side Effects Report #5574385-7
Physician from UNITED STATES reported HEPARIN problem on Dec 26, 2007. Female patient was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: device related infection, serratia bacteraemia, . HEPARIN dosage: unknown. Patient recovered.
DEVICE RELATED INFECTION : Enbrel Side Effects Report #5523471-6
ENBREL problem was reported by a Physician from UNITED STATES 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.
DEVICE RELATED INFECTION : Lioresal Side Effects Report #5525404-5
Physician from UNITED STATES reported LIORESAL problem 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.
DEVICE RELATED INFECTION : Fosamax Side Effects Report #5528500-1
FOSAMAX problem was reported by a Consumer or non-health professional from UNITED STATES 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.
DEVICE RELATED INFECTION : Natalizumab Side Effects Report #5531789-6
Consumer or non-health professional from UNITED STATES reported NATALIZUMAB problem 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.
DEVICE RELATED INFECTION : Bevacizumab Side Effects Report #5485114-X
BEVACIZUMAB problem was reported by a Consumer or non-health professional from UNITED STATES 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.
DEVICE RELATED INFECTION : Humira Side Effects Report #5490642-7
Consumer or non-health professional from UNITED KINGDOM reported HUMIRA problem 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.
DEVICE RELATED INFECTION : Temozolomide Side Effects Report #5473200-X
TEMOZOLOMIDE problem was reported by a Physician from UNITED KINGDOM 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.
DEVICE RELATED INFECTION : Prialt Side Effects Report #5407964-8
Consumer or non-health professional from UNITED STATES reported PRIALT problem 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.
DEVICE RELATED INFECTION : Humalog Side Effects Report #5427746-0
HUMALOG problem was reported by a Consumer or non-health professional from UNITED STATES 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : Premarin Side Effects Report #5678196-3
Consumer or non-health professional from UNITED STATES reported PREMARIN problem 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.
DEVICE RELATED INFECTION : Humira Side Effects Report #5620494-3
HUMIRA problem was reported by a Physician from GERMANY 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.
DEVICE RELATED INFECTION : Humira Side Effects Report #5628213-1
Consumer or non-health professional from BRAZIL reported HUMIRA problem on Feb 06, 2008. Female patient was diagnosed with rheumatoid arthritis, arrhythmia and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: anaemia, device related infection, knee arthroplasty, . HUMIRA dosage: unknown. During the same period patient was treated with SIMVASTATIN, DILTIAZEM, SPIRONOLACTONE, PREDNISONE, METHYLPREDNISOLONE. Patient was hospitalized. Patient recovered.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : 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.
DEVICE RELATED INFECTION : Peginterferon Side Effects Report #5679740-2
PEGINTERFERON ALFA problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 13, 2008. Male patient, child 12 years of age, weighting 55.12 lb, was diagnosed with metastases to lung and was treated with PEGINTERFERON ALFA. After drug was administered, patient experienced the following problems/side effects: arthritis bacterial, central line infection, device related infection, staphylococcal infection, . PEGINTERFERON ALFA dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE RELATED INFECTION : Humira Side Effects Report #5602777-6
Consumer or non-health professional from BRAZIL reported HUMIRA problem on Jan 17, 2008. Female patient, weighting 132.3 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthralgia, device migration, device related infection, fracture, . HUMIRA dosage: unknown. During the same period patient was treated with ETORICOXIB, DEFLAZACORT. Patient was hospitalized. Patient recovered.
DEVICE RELATED INFECTION : Cetuximab Side Effects Report #5545324-X
CETUXIMAB problem was reported by a Physician from UNITED STATES on Dec 07, 2007. Male patient, 47 years of age, weighting 138.0 lb, was diagnosed with neoplasm malignant and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: aortic valve incompetence, asthenia, device related infection, infusion site erythema, infusion site pain, infusion site swelling, staphylococcal infection, . CETUXIMAB dosage: 250MG/M2. During the same period patient was treated with TAXOL. Patient was hospitalized. Patient recovered.
DEVICE RELATED INFECTION : Lioresal Side Effects Report #5581107-2
Physician from UNITED STATES reported LIORESAL problem on Dec 19, 2007. Male patient, 14 years of age, was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, csf culture positive, device related infection, hyperhidrosis, hypertonia, meningitis, proteus infection, pseudomonas infection, . LIORESAL dosage: unknown. Patient recovered.
DEVICE RELATED INFECTION : Celecoxib Side Effects Report #5482692-1
CELECOXIB problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 28, 2007. Female patient was diagnosed with back disorder and was treated with CELECOXIB. After drug was administered, patient experienced the following problems/side effects: arthropathy, cerebrovascular accident, device related infection, diabetes mellitus, myocardial infarction, . CELECOXIB dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE RELATED INFECTION : Velcade Side Effects Report #5458127-1
Physician from GERMANY reported VELCADE problem on Sept 04, 2007. Female patient, 58 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: bronchitis, catheter related infection, device related infection, staphylococcal infection, . VELCADE dosage: unknown. During the same period patient was treated with DOXORUBICIN, DEXAMETHASONE, MELPHALAN, ACYCLOVIR, PANTOZOL. Patient was hospitalized. Patient recovered.
DEVICE RELATED INFECTION : Rebif Side Effects Report #5402122-5
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on July 13, 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: condition aggravated, depression, device related infection, meningitis bacterial, staphylococcal infection, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE RELATED INFECTION : Rebif Side Effects Report #5402122-5
Consumer or non-health professional from UNITED STATES reported REBIF problem on July 13, 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: condition aggravated, depression, device related infection, meningitis bacterial, staphylococcal infection, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.