DEVICE LEAKAGE side effect
What is DEVICE LEAKAGE ?Drugs associated with DEVICE LEAKAGE
AVONEX BETASERON BLEOMYCIN BYETTA CAVERJECT DIANEAL DURAGESIC EXTRANEAL FENTANYL FUZEON LEVEMIR NATALIZUMAB REVLIMID TRAVASOL ZANAFLEXDEVICE LEAKAGE : Fentanyl Side Effects Report #5648127-0
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Feb 22, 2008. Male patient, weighting 190.0 lb, was diagnosed with pain, back pain, sleep apnoea syndrome and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: device leakage, feeling abnormal, loss of consciousness, respiratory arrest, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, ACETAMINOPHEN AND OXYCODONE, DIAZEPAM, ROZEREM. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5650829-7
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 23, 2008. Male patient, weighting 155.0 lb, was diagnosed with bone pain, muscle spasms, osteoporosis, breakthrough pain, convulsion and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, hypogonadism, hypothyroidism, pain, . DURAGESIC dosage: unknown. During the same period patient was treated with BACLOFEN, BONIVA, IBUPROFEN, TYLENOL W, MORPHINE, ATIVAN, DIASTAT. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5671943-6
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Mar 11, 2008. Male patient, weighting 182.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, . DURAGESIC dosage: unknown. During the same period patient was treated with HYDROCODONE BITARTRATE. Patient died on 02/10/2005.
DEVICE LEAKAGE : Duragesic Side Effects Report #5673210-3
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 13, 2008. Male patient, weighting 182.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, . DURAGESIC dosage: unknown. During the same period patient was treated with HYDROCODONE BITARTRATE. Patient died on 02/10/2005.
DEVICE LEAKAGE : Dianeal Side Effects Report #5689329-7
Health Professional from UNITED STATES reported DIANEAL problem on Mar 21, 2008. Male patient was diagnosed with peritoneal dialysis and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: device leakage, . DIANEAL dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5627902-2
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 11, 2008. Male patient was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, . DURAGESIC dosage: unknown. During the same period patient was treated with HYDROCODONE BITARTRATE. Patient died on 02/10/2005.
DEVICE LEAKAGE : Extraneal Side Effects Report #5662560-2
Health Professional from UNITED STATES reported EXTRANEAL problem on Aug 31, 2007. Male patient, 74 years of age, weighting 260.0 lb, was diagnosed with renal disorder and was treated with EXTRANEAL. After drug was administered, patient experienced the following problems/side effects: device leakage, peritonitis bacterial, . EXTRANEAL dosage: unknown. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5586961-6
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 04, 2008. Male patient, weighting 176.4 lb, was diagnosed with pain, diabetes mellitus, depression, anxiety and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, narcotic intoxication, pruritus, urticaria, . DURAGESIC dosage: unknown. During the same period patient was treated with NORCO, AVANDIA, EFFEXOR, XANAX, WELLBUTRIN. Patient died on 10/02/2004.
DEVICE LEAKAGE : Dianeal Side Effects Report #5634302-8
Health Professional from UNITED STATES reported DIANEAL problem on Sept 07, 2007. Female patient, 50 years of age, was diagnosed with renal failure chronic and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: device leakage, peritonitis, . DIANEAL dosage: unknown. During the same period patient was treated with EXTRANEAL, EPOGEN, SENSIPAR, NEPHROCAPS. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Dianeal Side Effects Report #5634304-1
DIANEAL problem was reported by a Health Professional from UNITED STATES on Nov 20, 2007. Female patient, 52 years of age, was diagnosed with renal failure chronic and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: device leakage, dyspnoea, peritonitis, . DIANEAL dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Travasol Side Effects Report #5555848-7
Consumer or non-health professional from UNITED STATES reported TRAVASOL problem on Dec 06, 2007. Female patient was diagnosed with nutritional support and was treated with TRAVASOL. After drug was administered, patient experienced the following problems/side effects: device leakage, peritonitis bacterial, staphylococcal infection, therapeutic product contamination, . TRAVASOL dosage: unknown. During the same period patient was treated with PROSOL, STERILE WATERECTION IN PLASTIC CONTAINER. Patient recovered.
DEVICE LEAKAGE : Travasol Side Effects Report #5555938-9
TRAVASOL problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 06, 2007. Female patient was diagnosed with nutritional support and was treated with TRAVASOL. After drug was administered, patient experienced the following problems/side effects: device leakage, fungal peritonitis, therapeutic product contamination, . TRAVASOL dosage: unknown. During the same period patient was treated with PROSOL, STERILE WATER. Patient recovered.
DEVICE LEAKAGE : Fuzeon Side Effects Report #5557355-4
Consumer or non-health professional from UNITED STATES reported FUZEON problem on Nov 14, 2007. Male patient, 44 years of age, was treated with FUZEON. After drug was administered, patient experienced the following problems/side effects: device leakage, osteomyelitis, . FUZEON dosage: unknown. During the same period patient was treated with OMEPRAZOLE, SULFATRIM, DILANTIN, FLONASE, KALETRA, CLARITIN, FLOMAX, HYDROXYCHLOROQUINE SULPHATE. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5505352-7
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 25, 2007. Male patient, weighting 176.4 lb, was diagnosed with pain, diabetes mellitus, depression, anxiety, gastrooesophageal reflux disease and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, narcotic intoxication, pruritus, urticaria, . DURAGESIC dosage: unknown. During the same period patient was treated with NORCO, AVANDIA, EFFEXOR, XANAX, WELLBUTRIN, PEPCID. Patient died on 10/02/2004.
DEVICE LEAKAGE : Duragesic Side Effects Report #5514099-2
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Nov 05, 2007. Male patient, weighting 176.4 lb, was diagnosed with pain, diabetes mellitus, depression, anxiety and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, narcotic intoxication, pruritus, urticaria, . DURAGESIC dosage: unknown. During the same period patient was treated with NORCO, AVANDIA, EFFEXOR, XANAX, WELLBUTRIN. Patient died on 10/02/2004.
DEVICE LEAKAGE : Dianeal Side Effects Report #5523756-3
DIANEAL problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 16, 2007. Male patient, 52 years of age, weighting 178.6 lb, was diagnosed with peritoneal dialysis and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: device leakage, nausea, peritonitis bacterial, pyrexia, vomiting, . DIANEAL dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Bleomycin Side Effects Report #5533946-1
Physician from CANADA reported BLEOMYCIN problem on Nov 20, 2007. Female patient, child 5 years of age, was diagnosed with craniopharyngioma and was treated with BLEOMYCIN. After drug was administered, patient experienced the following problems/side effects: device leakage, diplopia, eyelid ptosis, fatigue, headache, hemiparesis, hydrocephalus, hypothalamo-pituitary disorder, lethargy, . BLEOMYCIN dosage: 3 MG 3/WK OTHER. During the same period patient was treated with CHLORIDE. Patient recovered.
DEVICE LEAKAGE : Dianeal Side Effects Report #5547466-1
DIANEAL problem was reported by a Health Professional from UNITED STATES on Apr 06, 2007. Male patient, 55 years of age, weighting 158.3 lb, was diagnosed with behcet's syndrome, renal failure chronic and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: device leakage, peritonitis bacterial, . DIANEAL dosage: unknown. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5487753-9
Pharmacist from UNITED KINGDOM reported DURAGESIC problem on Oct 05, 2007. Male patient was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, feeling abnormal, loss of consciousness, overdose, paralysis, . DURAGESIC dosage: unknown. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5492197-X
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 11, 2007. Male patient, weighting 176.4 lb, was diagnosed with pain, diabetes mellitus, depression, anxiety, gastrooesophageal reflux disease and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, narcotic intoxication, pruritus, urticaria, . DURAGESIC dosage: unknown. During the same period patient was treated with NORCO, AVANDIA, EFFEXOR, XANAX, WELLBUTRIN, PEPCID. Patient died on 10/02/2004.
DEVICE LEAKAGE : Duragesic Side Effects Report #5494900-1
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Oct 16, 2007. Male patient, weighting 176.4 lb, was diagnosed with pain, diabetes mellitus, depression, anxiety, gastrooesophageal reflux disease and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, narcotic intoxication, pruritus, urticaria, . DURAGESIC dosage: unknown. During the same period patient was treated with NORCO, AVANDIA, EFFEXOR, XANAX, WELLBUTRIN, PEPCID. Patient died on 10/02/2004.
DEVICE LEAKAGE : Duragesic Side Effects Report #5450016-1
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 05, 2007. Female patient, weighting 128.0 lb, was diagnosed with pain, breakthrough pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, disorientation, dyspnoea, feeling abnormal, heart rate abnormal, malaise, . DURAGESIC dosage: unknown. During the same period patient was treated with HYDROCODONE, FENTANYL. Patient recovered.
DEVICE LEAKAGE : Fentanyl Side Effects Report #5459402-7
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Sept 10, 2007. Female patient, weighting 140.0 lb, was diagnosed with back pain, gastrooesophageal reflux disease and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: device leakage, dysphagia, pain, palpitations, postnasal drip, somnolence, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with PROTONIX. Patient recovered.
DEVICE LEAKAGE : Caverject Side Effects Report #5473970-0
CAVERJECT problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 26, 2007. Male patient, 39 years of age, weighting 240.3 lb, was treated with CAVERJECT. After drug was administered, patient experienced the following problems/side effects: device leakage, . CAVERJECT dosage: unknown. During the same period patient was treated with REBIF, EFFEXOR, NEURONTIN, WELLBUTRIN, LITHIUM CARBONATE. Patient recovered.
DEVICE LEAKAGE : Fentanyl Side Effects Report #5420860-5
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Aug 06, 2007. Male patient was diagnosed with pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: device leakage, overdose, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. Patient died on 08/03/2005.
DEVICE LEAKAGE : Duragesic Side Effects Report #5425069-7
DURAGESIC problem was reported by a Physician from UNITED STATES on Aug 15, 2007. Male patient, weighting 255.0 lb, was diagnosed with local anaesthesia and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, overdose, respiratory failure, . DURAGESIC dosage: unknown. During the same period patient was treated with ALBUTEROL, FLOVENT, VIOXX, CEFAZOLIN, MARCAINE, LIDOCAINE W. Patient died on 07/10/2003.
DEVICE LEAKAGE : Fentanyl Side Effects Report #5379968-5
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on June 27, 2007. Female patient, weighting 138.0 lb, was diagnosed with pain, rheumatoid arthritis and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: device leakage, rheumatoid arthritis, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with PREDNISONE. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Natalizumab Side Effects Report #5398047-4
NATALIZUMAB problem was reported by a Physician from UNITED STATES on July 17, 2007. Female patient was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: device leakage, gastric disorder, stent related infection, urinary retention, . NATALIZUMAB dosage: 300 MG; QM; IV. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Fentanyl Side Effects Report #5379968-5
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on June 27, 2007. Female patient, weighting 138.0 lb, was diagnosed with pain, rheumatoid arthritis and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: device leakage, rheumatoid arthritis, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with PREDNISONE. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Natalizumab Side Effects Report #5398047-4
NATALIZUMAB problem was reported by a Physician from UNITED STATES on July 17, 2007. Female patient was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: device leakage, gastric disorder, stent related infection, urinary retention, . NATALIZUMAB dosage: 300 MG; QM; IV. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5672399-X
Health Professional from UNITED STATES reported DURAGESIC problem on Mar 18, 2008. Female patient, 45 years of age, weighting 180.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: breakthrough pain, device leakage, skin infection, skin irritation, thermal burn, underdose, withdrawal syndrome, . DURAGESIC dosage: unknown. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5683816-3
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 19, 2008. Female patient, weighting 175.0 lb, was diagnosed with pain, asthma, rheumatoid arthritis, breakthrough pain, thyroid disorder and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: compression fracture, device leakage, knee arthroplasty, pain, spinal compression fracture, . DURAGESIC dosage: unknown. During the same period patient was treated with FLOVENT, ALBUTEROL, PLAQUENIL, DAPRO, PREDNISONE, ULTRACET, THYROID. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5622030-4
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Jan 31, 2008. Female patient, weighting 145.0 lb, was diagnosed with pain, thyroid disorder, muscle spasms and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: autoimmune thyroiditis, device leakage, eye infection, loss of consciousness, muscle spasms, muscular weakness, pharyngeal neoplasm, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, LEVOTHYROXINE, LEVISON. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5624381-6
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 01, 2008. Female patient, weighting 200.0 lb, was diagnosed with pain in extremity, back pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: abscess limb, device leakage, heart rate increased, influenza, limb injury, motion sickness, palpitations, parosmia, . DURAGESIC dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Fentanyl Side Effects Report #5630171-0
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Feb 07, 2008. Male patient, weighting 280.0 lb, was diagnosed with pain, asthma, migraine, candidiasis, affective disorder, depression and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: blood testosterone decreased, device leakage, dry mouth, gastric ph decreased, hypertonic bladder, pulmonary embolism, pyrexia, sinusitis, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with ADVAIR DISKUS, ALBUTEROL, ATARAX, CLOTRIMAZOLE, SEROQUEL, SINGULAIR, TOPAMAX, CYMBALTA. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5632737-0
DURAGESIC problem was reported by a Physician from UNITED STATES on Feb 12, 2008. Female patient was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: device leakage, . DURAGESIC dosage: unknown. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5638750-1
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Feb 15, 2008. Female patient was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: chest discomfort, device leakage, dyspnoea, pain, . DURAGESIC dosage: unknown. Patient recovered.
DEVICE LEAKAGE : Zanaflex Side Effects Report #5512654-7
ZANAFLEX problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 01, 2007. Male patient was diagnosed with muscle spasticity and was treated with ZANAFLEX. After drug was administered, patient experienced the following problems/side effects: back pain, device leakage, dizziness, gait disturbance, hypertonia, hypoaesthesia, liver function test abnormal, muscle spasms, musculoskeletal stiffness, . ZANAFLEX dosage: unknown. During the same period patient was treated with BACLOFEN, KLONOCPIN. Patient recovered.
DEVICE LEAKAGE : Bleomycin Side Effects Report #5533958-8
Physician from CANADA reported BLEOMYCIN problem on Nov 20, 2007. Male patient, child 12 years of age, was diagnosed with craniopharyngioma and was treated with BLEOMYCIN. After drug was administered, patient experienced the following problems/side effects: cerebral cyst, device leakage, oedema, . BLEOMYCIN dosage: 3 MG 3/WK OTHER. During the same period patient was treated with CHLORIDE. Patient recovered.
DEVICE LEAKAGE : Betaseron Side Effects Report #5488884-X
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 04, 2007. Female patient, 34 years of age, was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: abdominal pain, device leakage, flatulence, gastrooesophageal reflux disease, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Levemir Side Effects Report #5441636-9
Health Professional from NETHERLANDS reported LEVEMIR problem on Aug 22, 2007. Male patient, 43 years of age, was diagnosed with type 1 diabetes mellitus and was treated with LEVEMIR. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, device leakage, hyperhidrosis, restlessness, . LEVEMIR dosage: unknown. During the same period patient was treated with NOVORAPID PENFILL. Patient recovered.
DEVICE LEAKAGE : Levemir Side Effects Report #5462682-5
LEVEMIR problem was reported by a Health Professional from NETHERLANDS on Sept 13, 2007. Male patient, 43 years of age, was diagnosed with type 1 diabetes mellitus and was treated with LEVEMIR. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, device leakage, hyperhidrosis, restlessness, . LEVEMIR dosage: unknown. During the same period patient was treated with NOVORAPID PENFILL. Patient recovered.
DEVICE LEAKAGE : Levemir Side Effects Report #5469292-4
Health Professional from NETHERLANDS reported LEVEMIR problem on Sept 21, 2007. Male patient, 43 years of age, was diagnosed with type 1 diabetes mellitus and was treated with LEVEMIR. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, device leakage, hyperhidrosis, restlessness, . LEVEMIR dosage: unknown. During the same period patient was treated with NOVORAPID PENFILL. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5375961-7
DURAGESIC problem was reported by a Pharmacist from UNITED STATES on June 21, 2007. Female patient, weighting 163.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: asthenia, device leakage, dizziness, fall, hypoaesthesia, hypotension, hypothyroidism, nausea, nodal arrhythmia, . DURAGESIC dosage: unknown. During the same period patient was treated with TIZANIDINE, ACTIQ, ROBAXIN, GABITRIL, NEURONTIN, HYDROCODONE BITARTRATE. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5375962-9
Physician from UNITED STATES reported DURAGESIC problem on June 22, 2007. Female patient, weighting 126.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: agitation, device leakage, hallucination, hyperkalaemia, ileus, overdose, therapeutic agent toxicity, urinary tract infection, . DURAGESIC dosage: unknown. During the same period patient was treated with CLONAZEPAM, LONOX, LORAZEPAM, LEVAQUIN. Patient was hospitalized. Patient died on 12/23/2003.
DEVICE LEAKAGE : Fentanyl Side Effects Report #5389916-X
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on July 09, 2007. Female patient, weighting 180.0 lb, was diagnosed with connective tissue disorder, blood pressure, pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: biopsy colon abnormal, device leakage, insomnia, jaw disorder, malaise, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, PREDNISONE, TENORMIN, PERCOCET, MORPHINE. Patient recovered.
DEVICE LEAKAGE : Avonex Side Effects Report #5398458-7
Consumer or non-health professional from UNITED STATES reported AVONEX problem on July 18, 2007. Female patient, 25 years of age, weighting 160.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: dehydration, device leakage, infection, . AVONEX dosage: unknown. During the same period patient was treated with BACLOFEN. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5375961-7
DURAGESIC problem was reported by a Pharmacist from UNITED STATES on June 21, 2007. Female patient, weighting 163.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: asthenia, device leakage, dizziness, fall, hypoaesthesia, hypotension, hypothyroidism, nausea, nodal arrhythmia, . DURAGESIC dosage: unknown. During the same period patient was treated with TIZANIDINE, ACTIQ, ROBAXIN, GABITRIL, NEURONTIN, HYDROCODONE BITARTRATE. Patient was hospitalized. Patient recovered.
DEVICE LEAKAGE : Duragesic Side Effects Report #5375962-9
Physician from UNITED STATES reported DURAGESIC problem on June 22, 2007. Female patient, weighting 126.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: agitation, device leakage, hallucination, hyperkalaemia, ileus, overdose, therapeutic agent toxicity, urinary tract infection, . DURAGESIC dosage: unknown. During the same period patient was treated with CLONAZEPAM, LONOX, LORAZEPAM, LEVAQUIN. Patient was hospitalized. Patient died on 12/23/2003.
DEVICE LEAKAGE : Fentanyl Side Effects Report #5389916-X
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on July 09, 2007. Female patient, weighting 180.0 lb, was diagnosed with connective tissue disorder, blood pressure, pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: biopsy colon abnormal, device leakage, insomnia, jaw disorder, malaise, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, PREDNISONE, TENORMIN, PERCOCET, MORPHINE. Patient recovered.
DEVICE LEAKAGE : Avonex Side Effects Report #5398458-7
Consumer or non-health professional from UNITED STATES reported AVONEX problem on July 18, 2007. Female patient, 25 years of age, weighting 160.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: dehydration, device leakage, infection, . AVONEX dosage: unknown. During the same period patient was treated with BACLOFEN. Patient was hospitalized. Patient recovered.