WOUND COMPLICATION side effect
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Drugs associated with WOUND COMPLICATION
ALTABAX ARIXTRA AVONEX BEVACIZUMAB CRESTOR FENTANYL FLUOCINOLONE HUMIRA LAPATINIB MICARDISFluocinolone Side Effects Report #5606701-1
Physician from UNITED STATES reported FLUOCINOLONE ACETONIDE INTRAVITREAL IMPLANT problem on Nov 05, 2007. Female patient, 63 years of age, was diagnosed with uveitis and was treated with FLUOCINOLONE ACETONIDE INTRAVITREAL IMPLANT. After drug was administered, patient experienced the following problems/side effects: endophthalmitis, wound complication, . FLUOCINOLONE ACETONIDE INTRAVITREAL IMPLANT dosage: unknown. During the same period patient was treated with FLUOCINOLONE ACETONIDE INTRAVITREAL IMPLANT, CELLCEPT. Patient recovered.
Avonex Side Effects Report #5510844-0
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 24, 2007. Female patient, 50 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: wound, wound complication, wound infection, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Fentanyl Side Effects Report #5661313-9
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Mar 03, 2008. Male patient, weighting 160.0 lb, was diagnosed with amputation, back pain, neuralgia, blood cholesterol, cardiac disorder, dyspepsia, hypertension and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: gangrene, wound complication, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, LIPITOR, PLETAL, PLAVIX, REGLAN, IMDUR, LOPRESSOR. Patient was hospitalized. Patient recovered.
Altabax Side Effects Report #5619725-5
ALTABAX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 02, 2008. Male patient, 65 years of age, weighting 150.4 lb, was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: application site discharge, application site erythema, wound complication, . ALTABAX dosage: unknown. Patient recovered.
Avonex Side Effects Report #5637933-4
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Feb 11, 2008. Female patient, 50 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: lethargy, osteomyelitis, wound complication, wound infection, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Micardis Side Effects Report #5571985-5
MICARDIS problem was reported by a Physician from JAPAN on Dec 20, 2007. Female patient, weighting 103.6 lb, was diagnosed with hypertension, headache and was treated with MICARDIS. After drug was administered, patient experienced the following problems/side effects: granulocyte count decreased, sepsis, wound complication, . MICARDIS dosage: unknown. During the same period patient was treated with VONFENAC. Patient recovered.
Arixtra Side Effects Report #5480450-5
Physician from JAPAN reported ARIXTRA problem on Oct 05, 2007. Female patient, 68 years of age, weighting 116.8 lb, was diagnosed with thrombosis prophylaxis, osteoporosis, procedural pain, conjunctivitis, insomnia and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: post procedural haematoma, post procedural swelling, wound complication, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with RISEDRONATE, HYPEN, MUCOSTA, FERROMIA, TARIVID, RHYTHMY, INDOMETHACIN, HARTMANNS. Patient was hospitalized. Patient recovered.
Arixtra Side Effects Report #5480566-3
ARIXTRA problem was reported by a Physician from JAPAN on Oct 05, 2007. Female patient, 68 years of age, weighting 116.8 lb, was diagnosed with thrombosis prophylaxis, osteoporosis, procedural pain, conjunctivitis, insomnia and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: post procedural haematoma, post procedural swelling, wound complication, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with RISEDRONATE, HYPEN, MUCOSTA, FERROMIA, TARIVID, RHYTHMY, INDOMETHACIN, HARTMANNS. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5768839-8
Physician from UNITED STATES reported HUMIRA problem on Apr 02, 2008. Male patient, weighting 158.1 lb, was diagnosed with ankylosing spondylitis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: perineal infection, procedural complication, wound complication, wound drainage, . HUMIRA dosage: unknown. Patient recovered.
Altabax Side Effects Report #5733697-4
ALTABAX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 15, 2008. Female patient, 35 years of age, was diagnosed with open wound and was treated with ALTABAX. After drug was administered, patient experienced the following problems/side effects: dermatitis contact, pain, wound complication, . ALTABAX dosage: unknown. During the same period patient was treated with MUPIROCIN. Patient recovered.
Lapatinib Side Effects Report #5709625-4
Physician from UNITED KINGDOM reported LAPATINIB problem on Apr 10, 2008. Female patient, 45 years of age, weighting 185.6 lb, was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: chills, postoperative wound infection, wound complication, . LAPATINIB dosage: 1250MG PER DAY. During the same period patient was treated with CAPECITABINE. Patient was hospitalized. Patient recovered.
Bevacizumab Side Effects Report #5373493-3
BEVACIZUMAB problem was reported by a Consumer or non-health professional from UNITED KINGDOM on June 14, 2007. Female patient, weighting 141.1 lb, was diagnosed with breast cancer metastatic and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: impaired healing, pneumocephalus, wound complication, . BEVACIZUMAB dosage: 960 MG, Q3W. During the same period patient was treated with MORPHINE. Patient was hospitalized. Patient died on 04/24/2007.
Crestor Side Effects Report #5241600-9
Consumer or non-health professional from UNITED STATES reported CRESTOR problem on Aug 12, 2005. Male patient, 58 years of age, weighting 172.0 lb, was diagnosed with blood cholesterol increased and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: dry skin, impaired healing, wound complication, . CRESTOR dosage: 20 MG PO. During the same period patient was treated with TENORMIN, LISINOPRIL. Patient recovered.