DEVICE MIGRATION side effect
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Drugs associated with DEVICE MIGRATION
AVONEX CEREZYME CISPLATIN COPPER DURAGESIC ETONOGESIREL ETONOGESTREL FENTANYL HUMIRA IMPLANON LIORESAL MIRENA MYOZYME NORPLANT PENTASA PREDNISOLONE TAXOLMirena Side Effects Report #5636017-9
Consumer or non-health professional from UNITED STATES reported MIRENA problem on Feb 20, 2008. Female patient, 25 years of age, weighting 224.0 lb, was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: device migration, pelvic pain, uterine rupture, . MIRENA dosage: unknown. Patient recovered.
Taxol Side Effects Report #5542596-2
TAXOL problem was reported by a Health Professional from UNITED STATES on Dec 05, 2007. Female patient, 48 years of age, was treated with TAXOL. After drug was administered, patient experienced the following problems/side effects: device migration, . TAXOL dosage: unknown. Patient was hospitalized. Patient recovered.
Implanon Side Effects Report #5450554-1
Physician from UNITED STATES reported IMPLANON problem on Aug 28, 2007. Female patient was treated with IMPLANON. After drug was administered, patient experienced the following problems/side effects: device migration, hysterectomy, . IMPLANON dosage: unknown. Patient recovered.
Pentasa Side Effects Report #5370592-7
PENTASA problem was reported by a Health Professional from ITALY on June 07, 2007. Female patient, 46 years of age, was diagnosed with colitis ulcerative and was treated with PENTASA. After drug was administered, patient experienced the following problems/side effects: device migration, erosive duodenitis, gastric ulcer, gastritis erosive, gastroduodenitis, vomiting, . PENTASA dosage: unknown. During the same period patient was treated with PANTOPRAZOLE, KETOROLAC TROMETHAMINE. Patient was hospitalized. Patient recovered.
Etonogesirel Side Effects Report #5273257-5
Consumer or non-health professional from FRANCE reported ETONOGESIREL problem on Mar 06, 2007. Female patient, 43 years of age, was treated with ETONOGESIREL. After drug was administered, patient experienced the following problems/side effects: device migration, implant site fibrosis, mobility decreased, musculoskeletal disorder, pain in extremity, paraesthesia, tendon disorder, . ETONOGESIREL dosage: unknown. Patient recovered.
Humira Side Effects Report #5602777-6
HUMIRA problem was reported by a Consumer or non-health professional from BRAZIL 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.
Implanon Side Effects Report #5604910-9
Physician from UNITED STATES reported IMPLANON problem on Jan 11, 2008. Female patient, 40 years of age, was treated with IMPLANON. After drug was administered, patient experienced the following problems/side effects: complication of device removal, device migration, hysterectomy, . IMPLANON dosage: unknown. Patient recovered.
Norplant Side Effects Report #5557498-5
NORPLANT SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 07, 2007. Female patient was diagnosed with contraception and was treated with NORPLANT SYSTEM. After drug was administered, patient experienced the following problems/side effects: complication of device removal, device migration, headache, pregnancy, . NORPLANT SYSTEM dosage: unknown. During the same period patient was treated with NORPLANT SYSTEM. Patient recovered.
Humira Side Effects Report #5504483-5
Consumer or non-health professional from BRAZIL reported HUMIRA problem on Oct 24, 2007. Female patient, weighting 196.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, device migration, headache, iliac artery occlusion, impaired healing, pain in extremity, postoperative wound infection, skin necrosis, . HUMIRA dosage: unknown. During the same period patient was treated with MAGISTRALMULA, FAMOTIDINE, CHLOROQUINE PHOSPHATE, FOLIC ACID, METHOTREXATE, NAPROXEN. Patient was hospitalized. Patient recovered.
Etonogestrel Side Effects Report #5482059-6
ETONOGESTREL problem was reported by a Consumer or non-health professional from AUSTRALIA on Sept 25, 2007. Female patient, 22 years of age, was diagnosed with contraception and was treated with ETONOGESTREL. After drug was administered, patient experienced the following problems/side effects: chest pain, device migration, paraesthesia, . ETONOGESTREL dosage: unknown. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5498097-3
Consumer or non-health professional from BRAZIL reported HUMIRA problem on Oct 15, 2007. Female patient, weighting 196.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, device migration, headache, iliac artery occlusion, impaired healing, pain in extremity, postoperative wound infection, skin necrosis, . HUMIRA dosage: unknown. During the same period patient was treated with MAGISTRALMULA, FAMOTIDINE, CHLOROQUINE PHOSPHATE, FOLIC ACID, METHOTREXATE, NAPROXEN. Patient was hospitalized. Patient recovered.
Cerezyme Side Effects Report #5465296-6
CEREZYME problem was reported by a Physician from UNITED STATES on Sept 13, 2007. Female patient, 82 years of age, weighting 127.9 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: coronary artery disease, device migration, dislocation of joint prosthesis, hip fracture, localised infection, myocardial infarction, sepsis, splenectomy, thrombocytopenia, . CEREZYME dosage: unknown. Patient died on 06/02/2007.
Cisplatin Side Effects Report #5418137-7
Health Professional from UNITED STATES reported CISPLATIN problem on July 31, 2007. Female patient, 43 years of age, was diagnosed with squamous cell carcinoma and was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: catheter related complication, device migration, peritonitis, . CISPLATIN dosage: unknown. During the same period patient was treated with ACTOS, TRAZODONE, PROTONIX, REGLAN, COLACE. Patient was hospitalized. Patient recovered.
Copper Side Effects Report #5383307-3
COPPER T problem was reported by a Physician from TUNISIA on June 22, 2007. Female patient, 42 years of age, was diagnosed with contraception and was treated with COPPER T. After drug was administered, patient experienced the following problems/side effects: calculus bladder, device migration, pregnancy with contraceptive device, uterine perforation, . COPPER T dosage: unknown. Patient recovered.
Prednisolone Side Effects Report #5403558-9
Consumer or non-health professional from UNITED KINGDOM reported PREDNISOLONE problem on July 13, 2007. Male patient, 42 years of age, was diagnosed with crohn's disease, hepatic haematoma and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: catheter related complication, device migration, haemodialysis, vascular rupture, . PREDNISOLONE dosage: unknown. During the same period patient was treated with HAEMOFILTRATION, WARFARIN. Patient recovered.
Copper Side Effects Report #5383307-3
COPPER T problem was reported by a Physician from TUNISIA on June 22, 2007. Female patient, 42 years of age, was diagnosed with contraception and was treated with COPPER T. After drug was administered, patient experienced the following problems/side effects: calculus bladder, device migration, pregnancy with contraceptive device, uterine perforation, . COPPER T dosage: unknown. Patient recovered.
Prednisolone Side Effects Report #5403558-9
Consumer or non-health professional from UNITED KINGDOM reported PREDNISOLONE problem on July 13, 2007. Male patient, 42 years of age, was diagnosed with crohn's disease, hepatic haematoma and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: catheter related complication, device migration, haemodialysis, vascular rupture, . PREDNISOLONE dosage: unknown. During the same period patient was treated with HAEMOFILTRATION, WARFARIN. Patient recovered.
Cerezyme Side Effects Report #5369687-3
CEREZYME problem was reported by a Physician from UNITED STATES on June 08, 2007. Female patient, weighting 127.9 lb, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: coronary artery disease, device migration, disease recurrence, dislocation of joint prosthesis, femur fracture, infection, myocardial infarction, sepsis, thrombocytopenia, . CEREZYME dosage: unknown. Patient died on 06/02/2007.
Myozyme Side Effects Report #5328162-2
Physician from ARGENTINA reported MYOZYME problem on Apr 30, 2007. Male patient, child 2 years of age, weighting 30.86 lb, was diagnosed with glycogen storage disease type ii and was treated with MYOZYME. After drug was administered, patient experienced the following problems/side effects: atelectasis, device migration, hypoxia, pyrexia, tracheal disorder, . MYOZYME dosage: 20 MG/KG Q2WKS IV. During the same period patient was treated with ALPHA, FLUTICASONE PROPIONATE, ALBUTEROL. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5302339-4
HUMIRA problem was reported by a Health Professional from UNITED KINGDOM on Apr 11, 2007. Female patient, weighting 116.8 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: dermal sinus, device migration, muscle operation, wound infection staphylococcal, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE, ALENDRONATE, CODEINE PHOSPHATE, ESTRADIOL, LOFEPRAMINE, MELOXICAM, PARACETAMOL, RABEPRAZOLE. Patient was hospitalized. Patient recovered.
Etonogestrel Side Effects Report #5313727-4
Consumer or non-health professional from GERMANY reported ETONOGESTREL problem on Apr 19, 2007. Female patient, 38 years of age, was treated with ETONOGESTREL. After drug was administered, patient experienced the following problems/side effects: breast cancer female, device migration, metastases to lymph nodes, . ETONOGESTREL dosage: unknown. Patient recovered.
Duragesic Side Effects Report #5664566-6
DURAGESIC problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 04, 2008. Female patient, weighting 100.0 lb, was diagnosed with pain, anxiety and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: convulsion, device migration, fall, limb operation, lower limb fracture, memory impairment, pain, tooth disorder, . DURAGESIC dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, LORAZEPAM. Patient was hospitalized. Patient recovered.
Fentanyl Side Effects Report #5679072-2
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Mar 14, 2008. Female patient, weighting 100.0 lb, was diagnosed with pain, anxiety and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: convulsion, device migration, fall, limb operation, lower limb fracture, memory impairment, pain, tooth disorder, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, LORAZEPAM. Patient was hospitalized. Patient recovered.
Prednisolone Side Effects Report #5413356-8
PREDNISOLONE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on July 25, 2007. Male patient, 42 years of age, was diagnosed with crohn's disease, hepatic haematoma and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: acute abdomen, continuous haemodiafiltration, device migration, haemodynamic instability, hepatic haematoma, intra-abdominal haematoma, oliguria, procedural complication, thrombosis in device, . PREDNISOLONE dosage: unknown. During the same period patient was treated with HAEMOFILTRATION, WARFARIN. Patient recovered.
Copper Side Effects Report #5383306-1
Physician from TUNISIA reported COPPER T problem on June 22, 2007. Female patient, 37 years of age, was diagnosed with contraception and was treated with COPPER T. After drug was administered, patient experienced the following problems/side effects: bladder perforation, calculus bladder, device migration, iatrogenic injury, iucd complication, urinary tract infection, uterine perforation, . COPPER T dosage: unknown. Patient recovered.
Copper Side Effects Report #5383306-1
COPPER T problem was reported by a Physician from TUNISIA on June 22, 2007. Female patient, 37 years of age, was diagnosed with contraception and was treated with COPPER T. After drug was administered, patient experienced the following problems/side effects: bladder perforation, calculus bladder, device migration, iatrogenic injury, iucd complication, urinary tract infection, uterine perforation, . COPPER T dosage: unknown. Patient recovered.
Avonex Side Effects Report #5305035-2
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Apr 04, 2007. Female patient, 44 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: abasia, condition aggravated, device migration, injury, muscle spasms, road traffic accident, sciatica, secondary progressive multiple sclerosis, spinal disorder, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Lioresal Side Effects Report #5286040-1
LIORESAL problem was reported by a Physician from UNITED STATES on Mar 23, 2007. Male patient was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: catheter related complication, device breakage, device migration, fall, muscle spasticity, . LIORESAL dosage: unknown. Patient recovered.