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ABDOMINAL ADHESIONS side effect

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Forteo Side Effects Report #5651089-3
Physician from UNITED STATES reported FORTEO problem on Feb 26, 2008. Female patient was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, arthralgia, muscular weakness, small intestinal obstruction, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5653586-3
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Physician from UNITED STATES on Feb 25, 2008. Female patient, weighting 166.0 lb, was diagnosed with pain, migraine, scoliosis, epilepsy, convulsion and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, abdominal pain upper, anxiety, application site discolouration, application site irritation, application site pruritus, application site rash, cardiac disorder, dehydration, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, DURAGESIC, GABITRIL, TOPAMAX, LIDODERM, IMITREX. Patient was hospitalized. Patient recovered.

Sildenafil Side Effects Report #5660958-X
Physician from UNITED KINGDOM reported SILDENAFIL problem on Feb 29, 2008. Male patient, weighting 15.43 lb, was diagnosed with lung disorder, pulmonary hypertension and was treated with SILDENAFIL. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, abdominal distension, bronchiolitis, fistula, gastrointestinal stoma complication, intestinal ischaemia, intestinal obstruction, . SILDENAFIL dosage: unknown. During the same period patient was treated with ANTIBIOTICS. Patient was hospitalized. Patient recovered.

Infliximab Side Effects Report #5675480-4
INFLIXIMAB problem was reported by a Health Professional from NETHERLANDS on Mar 12, 2008. Female patient, weighting 154.3 lb, was diagnosed with crohn's disease and was treated with INFLIXIMAB. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, peritonitis, sepsis, . INFLIXIMAB dosage: unknown. During the same period patient was treated with LANVIS, ENTOCORT EC, FOLIUM ZUMIR. Patient was hospitalized. Patient recovered.


Avonex Side Effects Report #5683518-3
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Mar 14, 2008. Female patient, 70 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, postoperative adhesion, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Mirena Side Effects Report #5683596-1
MIRENA problem was reported by a Physician from UNITED STATES on June 08, 2007. Female patient, 33 years of age, weighting 187.4 lb, was diagnosed with contraception and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, abdominal pain, procedural pain, uterine rupture, vaginal haemorrhage, . MIRENA dosage: unknown. Patient recovered.

Mirena Side Effects Report #5683638-3
Consumer or non-health professional from UNITED STATES reported MIRENA problem on Jan 17, 2007. Female patient, 34 years of age, weighting 202.8 lb, was diagnosed with contraception and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, complication of device insertion, pelvic peritoneal adhesions, procedural pain, uterine rupture, . MIRENA dosage: unknown. During the same period patient was treated with SYNTHROID, ZOCOR, BUMEX. Patient was hospitalized. Patient recovered.

Mirena Side Effects Report #5687741-3
MIRENA problem was reported by a Physician from UNITED STATES on June 08, 2007. Female patient, 33 years of age, weighting 187.4 lb, was diagnosed with contraception and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, abdominal pain, procedural pain, uterine rupture, vaginal haemorrhage, . MIRENA dosage: unknown. Patient recovered.

Mirena Side Effects Report #5687754-1
Consumer or non-health professional from UNITED STATES reported MIRENA problem on Jan 17, 2007. Female patient, 34 years of age, weighting 202.8 lb, was diagnosed with contraception and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, complication of device insertion, pelvic peritoneal adhesions, procedural pain, uterine rupture, . MIRENA dosage: unknown. During the same period patient was treated with SYNTHROID, ZOCOR, BUMEX. Patient was hospitalized. Patient recovered.


Fosamax Side Effects Report #5688721-4
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 19, 2008. Female patient, 68 years of age, weighting 110.2 lb, was diagnosed with osteoporosis, osteopenia, arthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, actinomycotic skin infection, angioedema, aortic calcification, arthralgia, bladder mass, bronchitis, catheter related infection, depression, . FOSAMAX dosage: unknown. During the same period patient was treated with SYNTHROID, AMBIEN, DELESTROGEN, VIOXX. Patient was hospitalized and became disabled. Patient recovered.

Fentanyl Side Effects Report #5612652-9
Physician from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Jan 22, 2008. Female patient, weighting 166.0 lb, was diagnosed with pain, migraine, scoliosis, epilepsy, convulsion and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, abdominal pain upper, anxiety, application site discolouration, application site irritation, application site pruritus, application site rash, cardiac disorder, dehydration, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, DURAGESIC, GABITRIL, TOPAMAX, LIDODERM, IMITREX. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5613970-0
FOSAMAX problem was reported by a Physician from UNITED STATES on Jan 25, 2008. Female patient, 68 years of age, weighting 110.2 lb, was diagnosed with osteoporosis, osteopenia, arthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, angioedema, aortic calcification, arthralgia, bladder mass, bronchitis, catheter related infection, depression, diabetes mellitus, . FOSAMAX dosage: unknown. During the same period patient was treated with SYNTHROID, AMBIEN, DELESTROGEN, VIOXX. Patient was hospitalized and became disabled. Patient recovered.

Femara Side Effects Report #5632281-0
Consumer or non-health professional from UNITED STATES reported FEMARA problem on Feb 12, 2008. Female patient, 51 years of age, weighting 125.0 lb, was diagnosed with metastases to bone and was treated with FEMARA. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, anaemia, blood albumin decreased, blood calcium decreased, blood creatinine abnormal, blood urea increased, breast cancer recurrent, focal glomerulosclerosis, haemodialysis, . FEMARA dosage: unknown. During the same period patient was treated with VOLTAREN, DYAZIDE, AREDIA, ARIMIDEX, ZOLOFT. Patient was hospitalized and became disabled. Patient recovered.

Prograf Side Effects Report #5636125-2
PROGRAF problem was reported by a Physician from COLOMBIA on Feb 08, 2008. Female patient, 39 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, intestinal obstruction, renal failure, . PROGRAF dosage: unknown. Patient died on 01/01/2008.


Fosamax Side Effects Report #5601416-8
Physician from UNITED STATES reported FOSAMAX problem on Jan 17, 2008. Female patient, 68 years of age, weighting 110.2 lb, was diagnosed with osteoporosis, osteopenia, arthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, angioedema, aortic calcification, arthralgia, bladder mass, bronchitis, catheter related infection, depression, diabetes mellitus, . FOSAMAX dosage: unknown. During the same period patient was treated with SYNTHROID, AMBIEN, DELESTROGEN, VIOXX. Patient was hospitalized and became disabled. Patient recovered.

Humira Side Effects Report #5601483-1
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 16, 2008. Female patient, weighting 103.1 lb, was diagnosed with crohn's disease and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, asthenia, gallbladder operation, headache, nausea, vomiting, . HUMIRA dosage: unknown. Patient was hospitalized. Patient recovered.

Cymbalta Side Effects Report #5606940-X
Consumer or non-health professional from UNITED STATES reported CYMBALTA problem on Jan 16, 2008. Male patient was diagnosed with pain in extremity, depression, sleep disorder, thrombosis, anxiety, back pain and was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, anxiety, crohn's disease, depression, gastrointestinal carcinoma, intestinal obstruction, intestinal polyp, malaise, . CYMBALTA dosage: 30 MG, DAILY (1/D). During the same period patient was treated with REMERON, SEROQUEL, GABAPENTIN, COUMADIN, PRILOSEC, XANAX, FLEXERIL. Patient was hospitalized. Patient recovered.

Lamictal Side Effects Report #5608951-7
LAMICTAL problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 29, 2008. Female patient, weighting 155.0 lb, was diagnosed with bipolar disorder and was treated with LAMICTAL. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, alopecia, balance disorder, blood disorder, depression, fibromyalgia, gait disturbance, immune system disorder, . LAMICTAL dosage: STARTED AT 25MG A DAY I WAS AT 200-300MG A DAY BY 1/19. Patient was hospitalized and became disabled. Patient recovered.

Avonex Side Effects Report #5610357-1
Health Professional from UNITED STATES reported AVONEX problem on Jan 16, 2008. Female patient, weighting 165.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, blood electrolytes decreased, blood pressure immeasurable, bradycardia, dehydration, depressed level of consciousness, diarrhoea, gastrointestinal gangrene, muscle spasticity, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.


Paragard Side Effects Report #5619478-0
PARAGARD T problem was reported by a Physician from UNITED STATES on Apr 03, 2007. Female patient, 34 years of age, weighting 188.0 lb, was diagnosed with contraception and was treated with PARAGARD T. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, abdominal pain, menorrhagia, ruptured ectopic pregnancy, . PARAGARD T dosage: unknown. During the same period patient was treated with ADVIL, VITAMIN. Patient was hospitalized. Patient recovered.

Sildenafil Side Effects Report #5537886-3
Physician from UNITED KINGDOM reported SILDENAFIL problem on Nov 29, 2007. Male patient, weighting 15.43 lb, was diagnosed with lung disorder and was treated with SILDENAFIL. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, abdominal distension, gastrointestinal stoma complication, intestinal ischaemia, intestinal obstruction, . SILDENAFIL dosage: unknown. During the same period patient was treated with ANTIBIOTICS. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5565127-X
ACCUTANE problem was reported by a Physician from UNITED STATES on Dec 11, 2007. Female patient, 15 years of age, weighting 128.1 lb, was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, acne, anorexia, arrhythmia, arthralgia, back pain, blood triglycerides increased, bulimia nervosa, cervical dysplasia, . ACCUTANE dosage: unknown. During the same period patient was treated with ORTHO TRI. Patient was hospitalized and became disabled. Patient recovered.

Avonex Side Effects Report #5567768-2
Physician from UNITED STATES reported AVONEX problem on Dec 06, 2007. Female patient, 59 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, benign gastrointestinal neoplasm, diverticulitis, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5572112-0
PROGRAF problem was reported by a Physician from UNITED STATES on Dec 05, 2007. Male patient, child 6 years of age, weighting 42.77 lb, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, bacteraemia, device occlusion, fungaemia, gastrointestinal necrosis, hydronephrosis, ileostomy closure, intestinal obstruction, klebsiella sepsis, . PROGRAF dosage: unknown. During the same period patient was treated with DACLIZUMAB, PREVACID, CLARITIN, CARBONATE. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5572168-5
Physician from UNITED STATES reported FOSAMAX problem on Dec 14, 2007. Female patient, 68 years of age, weighting 110.2 lb, was diagnosed with osteoporosis, osteopenia, arthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, angioedema, aortic calcification, arthralgia, bronchitis, catheter related infection, depression, diabetes mellitus, dyspnoea exertional, . FOSAMAX dosage: unknown. During the same period patient was treated with SYNTHROID, AMBIEN, DELESTROGEN, VIOXX. Patient was hospitalized and became disabled. Patient recovered.

Accutane Side Effects Report #5505041-9
ACCUTANE problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 26, 2007. Female patient, 15 years of age, weighting 128.1 lb, was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, acne, anorexia, arrhythmia, arthralgia, back pain, blood triglycerides increased, bulimia nervosa, cervical dysplasia, . ACCUTANE dosage: unknown. During the same period patient was treated with ORTHO TRI. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5505866-X
Physician from UNITED STATES reported FOSAMAX problem on Oct 23, 2007. Female patient, 68 years of age, weighting 110.2 lb, was diagnosed with osteoporosis, osteopenia, arthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, angioedema, aortic calcification, arthralgia, bronchitis, catheter related infection, depression, diabetes mellitus, dyspnoea exertional, . FOSAMAX dosage: unknown. During the same period patient was treated with SYNTHROID, AMBIEN, DELESTROGEN, VIOXX. Patient was hospitalized and became disabled. Patient recovered.

Natalizumab Side Effects Report #5506858-7
NATALIZUMAB problem was reported by a Health Professional from UNITED STATES on Oct 17, 2007. Female patient, 41 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, cholecystectomy, . NATALIZUMAB dosage: 300 MG;QM;IV. During the same period patient was treated with AVONEX. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5509048-7
Consumer or non-health professional from GERMANY reported AVONEX problem on Oct 18, 2007. Female patient, 44 years of age, weighting 156.5 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, alanine aminotransferase increased, aspartate aminotransferase increased, gamma-glutamyltransferase increased, hepatomegaly, ovarian cancer, ovarian cyst, salpingitis, tumour marker increased, . AVONEX dosage: unknown. During the same period patient was treated with RAMIPRIL HCT, AMLODIPINE. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5511029-4
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 29, 2007. Female patient, weighting 180.0 lb, was diagnosed with abdominal pain upper and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, condition aggravated, hiatus hernia, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, PERCOCET. Patient recovered.

Diclofenac Side Effects Report #5513510-0
Consumer or non-health professional from UNITED KINGDOM reported DICLOFENAC problem on Oct 25, 2007. Male patient, 40 years of age, was diagnosed with perineal pain and was treated with DICLOFENAC. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, gastrointestinal mucosal disorder, intestinal diaphragm disease, intestinal obstruction, intestinal polyp, intestinal ulcer perforation, mass, . DICLOFENAC dosage: 50 MG; TID; PO. Patient was hospitalized. Patient recovered.

Accutane Side Effects Report #5519283-X
ACCUTANE problem was reported by a Physician from UNITED STATES on Nov 09, 2007. Female patient, 15 years of age, weighting 128.1 lb, was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, acne, anorexia, arrhythmia, arthralgia, back pain, blood triglycerides increased, bulimia nervosa, cervical dysplasia, . ACCUTANE dosage: unknown. During the same period patient was treated with ORTHO TRI. Patient was hospitalized and became disabled. Patient recovered.

Fentanyl Side Effects Report #5522248-5
Consumer or non-health professional from UNITED STATES reported FENTANYL TRANSDERMAL SYSTEM problem on Nov 09, 2007. Female patient, weighting 166.0 lb, was diagnosed with pain, migraine, scoliosis, epilepsy, convulsion and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, abdominal pain upper, application site discolouration, application site irritation, application site pruritus, application site rash, cardiac disorder, dehydration, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, FENTANYL TRANSDERMAL SYSTEM, DURAGESIC, GABITRIL, TOPAMAX, LIDODERM, IMITREX. Patient was hospitalized. Patient recovered.

Natalizumab Side Effects Report #5523156-6
NATALIZUMAB problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 09, 2007. Female patient, 41 years of age, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, cholecystectomy, small intestinal obstruction, . NATALIZUMAB dosage: 300 MG; QM; IV. During the same period patient was treated with AVONEX. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5503530-4
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Oct 16, 2007. Female patient, 55 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5442629-8
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 adhesions, abdominal pain, abscess, adhesiolysis, c-reactive protein increased, central venous pressure decreased, colectomy, colitis, colostomy, . MYCOPHENOLATE MOFETIL dosage: 1 MG, BID. During the same period patient was treated with MYCOPHENOLATE MOFETIL, DECORTIN, TAZOBACTAM, VANCOMYCIN, METRONIDAZOLE, NEORAL, LIQUAEMIN. Patient was hospitalized. Patient died on 08/14/2007.

Fosamax Side Effects Report #5446921-2
Physician from UNITED STATES reported FOSAMAX problem on Aug 27, 2007. Female patient, 68 years of age, was diagnosed with osteoporosis, osteopenia, arthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, angioedema, aortic calcification, arthralgia, bronchitis, depression, diabetes mellitus, dyspnoea exertional, haemorrhoids, . FOSAMAX dosage: unknown. During the same period patient was treated with SYNTHROID, AMBIEN, DELESTROGEN, VIOXX. Patient was hospitalized and became disabled. Patient recovered.

Leuprolide Side Effects Report #5451803-6
LEUPROLIDE ACETATE problem was reported by a Consumer or non-health professional from JAPAN on Sept 10, 2007. Female patient, 36 years of age, was diagnosed with uterine leiomyoma and was treated with LEUPROLIDE ACETATE. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, ascites, blood creatine phosphokinase increased, . LEUPROLIDE ACETATE dosage: 3.75 MG (3.75 GM, 1 IN 28 D) SUBCUTANEOUS. Patient was hospitalized. Patient recovered.

Avastin Side Effects Report #5452716-6
Consumer or non-health professional from UNITED KINGDOM reported AVASTIN problem on Aug 30, 2007. Male patient, 53 years of age, weighting 141.1 lb, was diagnosed with colorectal cancer metastatic and was treated with AVASTIN. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, abdominal pain, diarrhoea, pyrexia, vomiting, . AVASTIN dosage: 325 MG, Q2W. During the same period patient was treated with AMARYL, LIPANTIL, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Copper Side Effects Report #5458173-8
COPPER IUD problem was reported by a Physician from UNITED KINGDOM on Sept 06, 2007. Female patient, 44 years of age, was diagnosed with contraception and was treated with COPPER IUD. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, abdominal strangulated hernia, actinomycosis, anorexia, cervicitis, device related infection, haemoglobin decreased, nausea, pelvic peritoneal adhesions, . COPPER IUD dosage: unknown. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5460715-3
Health Professional from UNITED STATES reported FOSAMAX problem on Sept 12, 2007. Female patient, 56 years of age, was diagnosed with osteoporosis prophylaxis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, anorgasmia, anxiety, appendicitis, biliary colic, chest discomfort, chest pain, cholecystitis chronic, dental caries, . FOSAMAX dosage: unknown. During the same period patient was treated with ACTONEL. Patient was hospitalized and became disabled. Patient recovered.

Dianeal Side Effects Report #5465911-7
DIANEAL problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 14, 2007. Female patient, 69 years of age, weighting 235.9 lb, was diagnosed with renal failure chronic and was treated with DIANEAL. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, appendicitis, catheter related complication, peritonitis bacterial, . DIANEAL dosage: unknown. Patient recovered.

Zelnorm Side Effects Report #5467750-X
Consumer or non-health professional from UNITED STATES reported ZELNORM problem on Sept 20, 2007. Female patient, 85 years of age, weighting 90.23 lb, was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, abdominal distension, abdominal hernia, abdominal pain, abdominal tenderness, acute prerenal failure, adhesiolysis, anaemia postoperative, anal sphincter atony, . ZELNORM dosage: 6 MG, BID. During the same period patient was treated with LOPRESSOR, DARVOCET, LEVSIN, VITAMIN CAP, CALCIUM, PRILOSEC, WARFARIN, FOSAMAX. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5472136-8
FOSAMAX problem was reported by a Physician from UNITED STATES on Sept 19, 2007. Female patient, 68 years of age, weighting 110.2 lb, was diagnosed with osteoporosis, osteopenia, arthritis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, angioedema, aortic calcification, arthralgia, bronchitis, catheter related infection, depression, diabetes mellitus, dyspnoea exertional, . FOSAMAX dosage: unknown. During the same period patient was treated with SYNTHROID, AMBIEN, DELESTROGEN, VIOXX. Patient was hospitalized and became disabled. Patient recovered.

Avonex Side Effects Report #5472294-5
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Sept 17, 2007. Female patient, 46 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, appendicitis perforated, cellulitis, diverticular perforation, muscle spasms, ovarian disorder, pelvic abscess, . AVONEX dosage: unknown. During the same period patient was treated with BACLOFEN, INTERFERON. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5408209-5
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 06, 2007. Female patient, weighting 156.5 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, infected lymphocele, neutrophil count decreased, small intestinal obstruction, white blood cell count decreased, . CISPLATIN dosage: 80 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, TAXOL. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5419140-3
Physician from GERMANY reported MYCOPHENOLATE MOFETIL problem on Aug 15, 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 adhesions, abdominal pain, abscess, adhesiolysis, c-reactive protein increased, colectomy, colitis, colostomy, cough, . 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 died on 08/14/2007.

Spiriva Side Effects Report #5421436-6
SPIRIVA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 20, 2007. Female patient, 67 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, gastrointestinal necrosis, obstruction, . SPIRIVA dosage: unknown. During the same period patient was treated with ASMANEX TWISTHALER, THEOPHYLLINE, VOSPIRE. Patient was hospitalized. Patient recovered.

Carboplatin Side Effects Report #5425909-1
Consumer or non-health professional from UNITED STATES reported CARBOPLATIN problem on Aug 23, 2007. Female patient, weighting 136.7 lb, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, activities of daily living impaired, constipation, haematoma, oral intake reduced, small intestinal obstruction, urinary tract infection enterococcal, . CARBOPLATIN dosage: 594 MG. During the same period patient was treated with TAXOL. Patient was hospitalized. Patient recovered.

Mycophenolate Side Effects Report #5430308-2
MYCOPHENOLATE MOFETIL problem was reported by a Physician from GERMANY on Aug 24, 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 adhesions, abdominal pain, abscess, adhesiolysis, c-reactive protein increased, central venous pressure decreased, colectomy, colitis, colostomy, . MYCOPHENOLATE MOFETIL dosage: 1 MG, BID. During the same period patient was treated with MYCOPHENOLATE MOFETIL, DECORTIN, TAZOBACTAM, VANCOMYCIN, METRONIDAZOLE, NEORAL, LIQUAEMIN. Patient was hospitalized. Patient died on 08/14/2007.

Humira Side Effects Report #5430684-0
Consumer or non-health professional from GERMANY reported HUMIRA problem on Aug 23, 2007. Female patient, weighting 136.7 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: abdominal adhesions, acute abdomen, gastrointestinal disorder, impaired healing, peritonitis, respiratory failure, small intestinal obstruction, staphylococcal infection, . HUMIRA dosage: unknown. During the same period patient was treated with CELECOXIB, PREDNISOLONE, METHOTREXATE, LEFLUNOMIDE, RUBIEFOL, CALCIMAGON D, PANTOPRAZOLE. Patient was hospitalized. Patient recovered.