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GRAFT COMPLICATION side effect

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Achilles Side Effects Report #5695383-9
Physician from UNITED STATES reported ACHILLES TENDON MUSCULOSKELETAL SOFT problem on Mar 14, 2008. Female patient, 42 years of age, was diagnosed with soft tissue injury and was treated with ACHILLES TENDON MUSCULOSKELETAL SOFT. After drug was administered, patient experienced the following problems/side effects: graft complication, incision site pain, oedema peripheral, synovial cyst, . ACHILLES TENDON MUSCULOSKELETAL SOFT dosage: unknown. During the same period patient was treated with STAPLE. Patient recovered.

Flex Side Effects Report #5631705-2
FLEX HD problem was reported by a Physician from UNITED STATES on Jan 18, 2008. Female patient was diagnosed with soft tissue disorder and was treated with FLEX HD. After drug was administered, patient experienced the following problems/side effects: graft complication, graft infection, incision site erythema, incision site oedema, necrosis, post procedural discharge, staphylococcal infection, . FLEX HD dosage: unknown. During the same period patient was treated with FLEX HD. Patient was hospitalized. Patient recovered.

Skin Side Effects Report #5649840-1
Physician from UNITED STATES reported SKIN problem on Jan 18, 2008. Female patient was diagnosed with soft tissue disorder and was treated with SKIN. After drug was administered, patient experienced the following problems/side effects: graft complication, graft infection, incision site erythema, post procedural swelling, staphylococcal infection, wound secretion, . SKIN dosage: unknown. Patient was hospitalized. Patient recovered.

Celebrex Side Effects Report #5609117-7
CELEBREX problem was reported by a Health Professional from UNITED STATES on Jan 30, 2008. Female patient, weighting 148.0 lb, was diagnosed with arthralgia and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: graft complication, necrosis, . CELEBREX dosage: 200 MG 1 PER DAY ORAL. Patient was hospitalized and became disabled. Patient recovered.


Femoral Side Effects Report #5544515-1
Physician from UNITED STATES reported FEMORAL HEAD FZ problem on Nov 05, 2007. Female patient, 25 years of age, was diagnosed with transplant and was treated with FEMORAL HEAD FZ. After drug was administered, patient experienced the following problems/side effects: graft complication, post procedural infection, . FEMORAL HEAD FZ dosage: unknown. During the same period patient was treated with TIBIALIS TENDON. Patient was hospitalized. Patient recovered.

Semitendinosus Side Effects Report #5486724-6
SEMITENDINOSUS TENDON problem was reported by a Health Professional from UNITED STATES on Oct 12, 2007. Female patient was diagnosed with soft tissue disorder, surgery and was treated with SEMITENDINOSUS TENDON. After drug was administered, patient experienced the following problems/side effects: graft complication, pyrexia, . SEMITENDINOSUS TENDON dosage: unknown. During the same period patient was treated with SEMITENDINOSUS TENDON. Patient was hospitalized. Patient recovered.

Eye Side Effects Report #5507225-2
Physician from UNITED STATES reported EYE problem on Sept 24, 2007. Male patient, 63 years of age, was diagnosed with fuchs' syndrome and was treated with EYE. After drug was administered, patient experienced the following problems/side effects: graft complication, . EYE dosage: unknown. Patient recovered.

Semitendinosus Side Effects Report #5719246-5
SEMITENDINOSUS TENDON problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 25, 2008. Male patient, 22 years of age, was diagnosed with soft tissue disorder, therapeutic procedure and was treated with SEMITENDINOSUS TENDON. After drug was administered, patient experienced the following problems/side effects: graft complication, unevaluable event, . SEMITENDINOSUS TENDON dosage: unknown. During the same period patient was treated with SEMITENDINOSUS TENDON, SEMITENDINOSUS TENDON, SEMITENDINOSUS TENDON. Patient was hospitalized. Patient recovered.

Carticel Side Effects Report #5326579-3
Physician from UNITED STATES reported CARTICEL problem on Apr 27, 2007. Female patient was diagnosed with chondropathy and was treated with CARTICEL. After drug was administered, patient experienced the following problems/side effects: graft complication, procedural pain, treatment noncompliance, . CARTICEL dosage: unknown. Patient recovered.


Betamethasone Side Effects Report #5622963-9
BETAMETHASONE PHOSPHATE problem was reported by a Physician from JAPAN on Jan 25, 2008. Female patient, 85 years of age, was diagnosed with procedural site reaction and was treated with BETAMETHASONE PHOSPHATE. After drug was administered, patient experienced the following problems/side effects: calcinosis, graft complication, . BETAMETHASONE PHOSPHATE dosage: unknown. During the same period patient was treated with CRAVIT. Patient recovered.

Diovan Side Effects Report #5479241-0
Consumer or non-health professional from MEXICO reported DIOVAN HCT problem on Sept 27, 2007. Female patient, 77 years of age, was diagnosed with hypertension and was treated with DIOVAN HCT. After drug was administered, patient experienced the following problems/side effects: accident, graft complication, skin graft, . DIOVAN HCT dosage: 160/12.5MG DAILY. Patient was hospitalized. Patient recovered.

Hemi Side Effects Report #5507228-8
HEMI PATELLAR LIGAMENT problem was reported by a Health Professional from UNITED STATES on Sept 24, 2007. Male patient, 19 years of age, was diagnosed with ligament operation and was treated with HEMI PATELLAR LIGAMENT. After drug was administered, patient experienced the following problems/side effects: culture positive, graft complication, staphylococcal infection, . HEMI PATELLAR LIGAMENT dosage: unknown. Patient was hospitalized. Patient recovered.

Sirolimus Side Effects Report #5463332-4
Health Professional from EGYPT reported SIROLIMUS problem on Sept 10, 2007. Female patient, 37 years of age, was treated with SIROLIMUS. After drug was administered, patient experienced the following problems/side effects: focal glomerulosclerosis, graft complication, . SIROLIMUS dosage: unknown. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISONE, BASILIXIMAB. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5761236-0
MYFORTIC problem was reported by a Physician from SPAIN on June 03, 2008. Female patient was diagnosed with renal transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: biopsy kidney, graft complication, microangiopathic haemolytic anaemia, nephropathy toxic, renal tubular necrosis, thrombocytopenia, . MYFORTIC dosage: unknown. During the same period patient was treated with TACROLIMUS COMP, TACROLIMUS COMP. Patient was hospitalized. Patient recovered.


Avonex Side Effects Report #5745929-7
Consumer or non-health professional from UNITED STATES reported AVONEX problem on May 06, 2008. Female patient, 57 years of age, weighting 152.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: acute coronary syndrome, graft complication, myocardial infarction, post procedural complication, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Myfortic Side Effects Report #5754110-7
MYFORTIC problem was reported by a Physician from SPAIN on May 28, 2008. Female patient was diagnosed with renal transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: biopsy kidney, graft complication, microangiopathic haemolytic anaemia, nephropathy toxic, renal tubular necrosis, thrombocytopenia, . MYFORTIC dosage: unknown. During the same period patient was treated with TACROLIMUS COMP, TACROLIMUS COMP. Patient was hospitalized. Patient recovered.

Skin Side Effects Report #5705196-7
Consumer or non-health professional from UNITED STATES reported SKIN problem on Mar 14, 2008. Female patient was diagnosed with thermal burn and was treated with SKIN. After drug was administered, patient experienced the following problems/side effects: blood culture positive, graft complication, serratia infection, . SKIN dosage: unknown. Patient recovered.

Skin Side Effects Report #5369003-7
SKIN problem was reported by a Physician from UNITED STATES on Apr 24, 2007. Female patient, 58 years of age, was treated with SKIN. After drug was administered, patient experienced the following problems/side effects: excessive granulation tissue, graft complication, inflammation, wound drainage, . SKIN dosage: unknown. Patient recovered.

Carticel Side Effects Report #5341330-9
Consumer or non-health professional from GERMANY reported CARTICEL problem on May 16, 2007. Female patient, 14 years of age, was diagnosed with arthropathy and was treated with CARTICEL. After drug was administered, patient experienced the following problems/side effects: chondromatosis, graft complication, . CARTICEL dosage: unknown. Patient recovered.


Amifostine Side Effects Report #5295662-3
AMIFOSTINE problem was reported by a Health Professional from UNITED STATES on Apr 10, 2007. Male patient, 52 years of age, weighting 149.0 lb, was diagnosed with neoplasm malignant and was treated with AMIFOSTINE. After drug was administered, patient experienced the following problems/side effects: eye swelling, graft complication, ocular hyperaemia, pruritus, rash maculo-papular, . AMIFOSTINE dosage: 500 MG SQ DAILY M-F X 18 DAY. During the same period patient was treated with RADIATION. Patient recovered.

Phenytoin Side Effects Report #5549835-2
Pharmacist from UNITED STATES reported PHENYTOIN problem on Dec 07, 2007. Female patient, 52 years of age, was diagnosed with convulsion prophylaxis and was treated with PHENYTOIN. After drug was administered, patient experienced the following problems/side effects: body temperature fluctuation, condition aggravated, graft complication, hepatotoxicity, hypotension, hypothermia, skin disorder, skin graft, toxic epidermal necrolysis, . PHENYTOIN dosage: 300MG DAILY PO. Patient died on 12/04/2007.

Musculoskeletal Side Effects Report #5468089-9
MUSCULOSKELETAL SOFT problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 12, 2007. Female patient, 28 years of age, was treated with MUSCULOSKELETAL SOFT. After drug was administered, patient experienced the following problems/side effects: complications of transplant surgery, failure of implant, graft complication, . MUSCULOSKELETAL SOFT dosage: unknown. Patient recovered.

Carticel Side Effects Report #5376068-5
Physician from UNITED STATES reported CARTICEL problem on July 02, 2007. Female patient, 34 years of age, was diagnosed with arthropathy and was treated with CARTICEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, chondromalacia, graft complication, graft delamination, loose body in joint, osteochondrosis, . CARTICEL dosage: unknown. Patient recovered.

Carticel Side Effects Report #5376068-5
CARTICEL problem was reported by a Physician from UNITED STATES on July 02, 2007. Female patient, 34 years of age, was diagnosed with arthropathy and was treated with CARTICEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, chondromalacia, graft complication, graft delamination, loose body in joint, osteochondrosis, . CARTICEL dosage: unknown. Patient recovered.

Carticel Side Effects Report #5748480-3
Physician from UNITED STATES reported CARTICEL problem on Apr 14, 2008. Male patient, 38 years of age, was diagnosed with arthropathy and was treated with CARTICEL. After drug was administered, patient experienced the following problems/side effects: bursitis, cartilage injury, graft complication, hypotonia, joint effusion, loose body in joint, synovitis, . CARTICEL dosage: unknown. During the same period patient was treated with PEGASYS. Patient recovered.

Vexol Side Effects Report #5362799-X
VEXOL problem was reported by a Consumer or non-health professional from FRANCE on May 31, 2007. Male patient, 24 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with VEXOL. After drug was administered, patient experienced the following problems/side effects: astigmatism, graft complication, ocular hypertension, suture rupture, . VEXOL dosage: unknown. Patient recovered.

Myfortic Side Effects Report #5290692-X
Pharmacist from UNITED STATES reported MYFORTIC problem on Apr 05, 2007. Male patient, 39 years of age, weighting 186.1 lb, was diagnosed with immunosuppression, renal and pancreas transplant and was treated with MYFORTIC. After drug was administered, patient experienced the following problems/side effects: abdominal pain, diarrhoea, graft complication, nausea, vomiting, . MYFORTIC dosage: 180MG PO TID. During the same period patient was treated with VALGANCICLOVIR, TACROLIMUS, METOCLOPRAMIDE, LANSOPRAZOLE, PREDNISONE, NYSTATIN, INSULIN. Patient was hospitalized. Patient recovered.

Vexol Side Effects Report #5266714-9
VEXOL problem was reported by a Health Professional from FRANCE on Feb 26, 2007. Male patient, 24 years of age, was treated with VEXOL. After drug was administered, patient experienced the following problems/side effects: astigmatism, graft complication, ocular hypertension, suture rupture, . VEXOL dosage: unknown. Patient recovered.