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ADHESIOLYSIS side effect

What is ADHESIOLYSIS ?
Help Community - Describe Your Side Effect   Search FDA Side Effects   Ask Health Expert   ADHESIOLYSIS and Recently Reported Side Effects   ADHESIOLYSIS and 15 most Active Side Effect polls   ADHESIOLYSIS and featured health surveys   Substances toxic to Health   Recent Hospital reviews   Comments about Side Effects   Hospital Quality reviews   Homecare Quality reviews
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Drugs associated with ADHESIOLYSIS

CARBOPLATIN  COUMADIN  ESTRADERM  GLEEVEC  IUS  LIPITOR  MYCOPHENOLATE  RAD  RALOXIFENE  REMICADE  


Raloxifene Side Effects Report #5493101-0
Physician from KOREA, REPUBLIC OF reported RALOXIFENE HYDROCHLORIDE problem on Oct 09, 2007. Female patient, weighting 132.3 lb, was diagnosed with osteoporosis and was treated with RALOXIFENE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: adhesiolysis, . RALOXIFENE HYDROCHLORIDE dosage: 60 MG, DAILY (1/D). Patient was hospitalized. Patient recovered.

Carboplatin Side Effects Report #5426055-3
CARBOPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 24, 2007. Female patient, weighting 120.2 lb, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: adhesiolysis, failure to thrive, nausea, small intestinal obstruction, vomiting, . CARBOPLATIN dosage: 738 MG. During the same period patient was treated with TAXOTERE, TAXOL. Patient was hospitalized. Patient recovered.

Rad Side Effects Report #5772304-1
Physician from GERMANY reported RAD problem on June 11, 2008. Male patient, weighting 264.6 lb, was diagnosed with heart transplant and was treated with RAD. After drug was administered, patient experienced the following problems/side effects: adhesiolysis, anastomotic complication, gastrointestinal necrosis, haemodynamic instability, immunosuppression, intestinal resection, large intestine perforation, leukopenia, mediastinitis, . RAD dosage: 0.5 MG, BID. During the same period patient was treated with SANDIMMUNE, PREDNISOLONE. Patient died on 06/06/2008.

Rad Side Effects Report #5752580-1
RAD problem was reported by a Physician from GERMANY on May 23, 2008. Male patient, weighting 264.6 lb, was diagnosed with heart transplant and was treated with RAD. After drug was administered, patient experienced the following problems/side effects: adhesiolysis, anastomotic complication, intestinal resection, large intestine perforation, leukopenia, mediastinitis, peritonitis, sternal wiring, . RAD dosage: 0.5 MG, BID. During the same period patient was treated with SANDIMMUNE, PREDNISOLONE. Patient recovered.


Ius Side Effects Report #5622688-X
Physician from HUNGARY reported IUS SHG problem on Jan 30, 2008. Female patient, 37 years of age, was diagnosed with contraception and was treated with IUS SHG. After drug was administered, patient experienced the following problems/side effects: abdominal pain, adhesiolysis, . IUS SHG dosage: unknown. Patient was hospitalized. Patient recovered.

Ius Side Effects Report #5625564-1
IUS SHG problem was reported by a Physician from HUNGARY on Jan 30, 2008. Female patient, 37 years of age, was diagnosed with contraception and was treated with IUS SHG. After drug was administered, patient experienced the following problems/side effects: abdominal pain, adhesiolysis, . IUS SHG dosage: unknown. Patient was hospitalized. Patient recovered.

Coumadin Side Effects Report #5564306-5
Consumer or non-health professional from UNITED STATES reported COUMADIN problem on Dec 14, 2007. Female patient, 52 years of age, weighting 220.0 lb, was diagnosed with thrombosis prophylaxis, gout and was treated with COUMADIN. After drug was administered, patient experienced the following problems/side effects: abscess, adhesiolysis, altered state of consciousness, alveoloplasty, back pain, bacterial infection, bone disorder, bone neoplasm malignant, cardiac failure congestive, . COUMADIN dosage: 7.5 MG, QD. During the same period patient was treated with ALLOPURINOL, POTASSIUM CHLORIDE, PROTONIX, ALDACTONE, ALPRAZOLAM, FERROUS SULPHATE, INTERFERON. Patient was hospitalized. Patient recovered.

Lipitor Side Effects Report #5352010-8
LIPITOR problem was reported by a Consumer or non-health professional from UNITED STATES on May 29, 2007. Female patient, 38 years of age, weighting 140.0 lb, was diagnosed with blood cholesterol increased, hypertension and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: abdominal pain, adhesiolysis, asthma, back pain, blood potassium decreased, blood pressure decreased, bowel sounds abnormal, cataract operation, catheterisation cardiac, . LIPITOR dosage: unknown. During the same period patient was treated with METOPROLOL SUCCINATE, METOPROLOL SUCCINATE, PLAVIX, ASPIRIN, LISINOPRIL, WELLBUTRIN, PROZAC, DIAZEPAM. Patient was hospitalized. Patient recovered.

Coumadin Side Effects Report #5366469-3
Consumer or non-health professional from UNITED STATES reported COUMADIN problem on June 18, 2007. Female patient, 52 years of age, weighting 220.0 lb, was diagnosed with thrombosis prophylaxis, gout and was treated with COUMADIN. After drug was administered, patient experienced the following problems/side effects: abscess, adhesiolysis, alveoloplasty, back pain, bacterial infection, bone disorder, bone neoplasm malignant, cardiac failure congestive, depressed level of consciousness, . COUMADIN dosage: 7.5 MG, QD. During the same period patient was treated with ALLOPURINOL, POTASSIUM ACETATE, PROTONIX, ALDACTONE, ALPRAZOLAM, FERROUS SULPHATE, INTERFERON. Patient was hospitalized. Patient recovered.


Lipitor Side Effects Report #5334369-0
LIPITOR problem was reported by a Consumer or non-health professional from UNITED STATES on May 16, 2007. Female patient, 38 years of age, weighting 140.0 lb, was diagnosed with blood cholesterol increased, hypertension and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: abdominal pain, adhesiolysis, blood potassium decreased, blood pressure decreased, bowel sounds abnormal, catheterisation cardiac, chest pain, cholecystectomy, cholelithiasis, . LIPITOR dosage: unknown. During the same period patient was treated with METOPROLOL SUCCINATE, METOPROLOL SUCCINATE, PLAVIX, ASPIRIN, LISINOPRIL, WELLBUTRIN, PROZAC, DIAZEPAM. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5298723-8
Health Professional from CANADA reported REMICADE problem on Apr 09, 2007. Male patient, 53 years of age, was diagnosed with crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: acute pulmonary oedema, adhesiolysis, cellulitis, haemoglobin decreased, necrotising fasciitis, nephrolithiasis, pneumocystis jiroveci pneumonia, pneumonia bacterial, . REMICADE dosage: unknown. During the same period patient was treated with STEROIDS. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5657353-6
GLEEVEC problem was reported by a Consumer or non-health professional from JAPAN on Mar 05, 2008. Male patient, 66 years of age, weighting 145.5 lb, was diagnosed with gastrointestinal stromal tumour and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abdominal wall disorder, adhesiolysis, anaemia, ascites, blood pressure decreased, c-reactive protein increased, gastrectomy, . GLEEVEC dosage: 400 MG/DAY. Patient was hospitalized. Patient died on 10/26/2007.

Gleevec Side Effects Report #5675716-X
Consumer or non-health professional from JAPAN reported GLEEVEC problem on Mar 17, 2008. Male patient, 66 years of age, weighting 145.5 lb, was diagnosed with gastrointestinal stromal tumour and was treated with GLEEVEC. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abdominal wall disorder, adhesiolysis, anaemia, ascites, blood alkaline phosphatase increased, blood pressure decreased, c-reactive protein increased, gastrectomy, . GLEEVEC dosage: 400 MG/DAY. Patient was hospitalized. Patient died on 10/26/2007.

Estraderm Side Effects Report #5528976-X
ESTRADERM problem was reported by a Consumer or non-health professional from UNITED STATES on June 08, 2007. Female patient, 60 years of age, weighting 132.9 lb, was diagnosed with menopause and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: abdominal pain, adenomyosis, adhesiolysis, anxiety, breast cancer, breast mass, breast reconstruction, cholangiogram abnormal, cholecystectomy, . ESTRADERM dosage: 0.05 MG, TRANSDERMAL. During the same period patient was treated with PREMARIN, PROVERA, MEDROXYPROGESTERONE ACETATE, MEDROXYPROGESTERONE ACETATE, MEDROXYPROGESTERONE ACETATE, PREMPRO. Patient recovered.


Mycophenolate Side Effects Report #5405683-5
Physician from GERMANY reported MYCOPHENOLATE MOFETIL problem on July 27, 2007. Male patient, 50 years of age, weighting 158.7 lb, was diagnosed with heart transplant, bronchitis, thrombosis prophylaxis and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abscess, adhesiolysis, colectomy, colitis, ileus, infection, intestinal haemorrhage, laparotomy, . MYCOPHENOLATE MOFETIL dosage: 1 MG, BID. During the same period patient was treated with MYCOPHENOLATE MOFETIL, DECORTIN, TAZOBAC, VANCOMYCIN, METRONIDAZOLE, NEORAL, HEPARIN. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5408042-4
MYCOPHENOLATE MOFETIL problem was reported by a Physician from GERMANY on Aug 03, 2007. Male patient, 50 years of age, weighting 158.7 lb, was diagnosed with heart transplant, bronchitis, thrombosis prophylaxis and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abscess, adhesiolysis, colectomy, colitis, ileus, infection, intestinal haemorrhage, laparotomy, . MYCOPHENOLATE MOFETIL dosage: 1 MG, BID. During the same period patient was treated with MYCOPHENOLATE MOFETIL, DECORTIN, TAZOBAC, VANCOMYCIN, METRONIDAZOLE, NEORAL, HEPARIN. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5399829-5
Physician from GERMANY reported MYCOPHENOLATE MOFETIL problem on July 23, 2007. Male patient, 50 years of age, weighting 158.7 lb, was diagnosed with heart transplant, bronchitis and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abscess, adhesiolysis, colectomy, colitis, ileus, infection, intestinal haemorrhage, laparotomy, . MYCOPHENOLATE MOFETIL dosage: 1 MG, BID. During the same period patient was treated with MYCOPHENOLATE MOFETIL, DECORTIN, TAZOBAC, VANCOMYCIN, METRONIDAZOLE, NEORAL. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5399829-5
MYCOPHENOLATE MOFETIL problem was reported by a Physician from GERMANY on July 23, 2007. Male patient, 50 years of age, weighting 158.7 lb, was diagnosed with heart transplant, bronchitis and was treated with MYCOPHENOLATE MOFETIL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, abscess, adhesiolysis, colectomy, colitis, ileus, infection, intestinal haemorrhage, laparotomy, . MYCOPHENOLATE MOFETIL dosage: 1 MG, BID. During the same period patient was treated with MYCOPHENOLATE MOFETIL, DECORTIN, TAZOBAC, VANCOMYCIN, METRONIDAZOLE, NEORAL. Patient was hospitalized. Patient recovered.

Estraderm Side Effects Report #5786109-9
Consumer or non-health professional from UNITED STATES reported ESTRADERM problem on June 09, 2008. Female patient, weighting 133.0 lb, was diagnosed with menopause, hot flush, prophylaxis and was treated with ESTRADERM. After drug was administered, patient experienced the following problems/side effects: abdominal pain, adenomyosis, adhesiolysis, anxiety, breast cancer, breast mass, breast reconstruction, cholangiogram abnormal, cholecystectomy, . ESTRADERM dosage: 0.05 MG, UNK. During the same period patient was treated with PREMARIN, PROVERA. Patient recovered.


Coumadin Side Effects Report #5258370-0
COUMADIN problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 23, 2007. Female patient, 52 years of age, weighting 220.0 lb, was diagnosed with thrombosis prophylaxis, gout and was treated with COUMADIN. After drug was administered, patient experienced the following problems/side effects: abdominal wall infection, abscess, adhesiolysis, alveoloplasty, back pain, bacterial infection, bone disorder, bone neoplasm malignant, cardiac failure congestive, . COUMADIN dosage: 7.5 MG, QD. During the same period patient was treated with ALLOPURINOL, POTASSIUM ACETATE, PROTONIX, ALDACTONE, ALPRAZOLAM, FERROUS SULPHATE, INTERFERON. Patient was hospitalized. Patient recovered.

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