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FEEDING DISORDER side effect

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Oxcarbazepine Side Effects Report #5657926-0
Consumer or non-health professional from UNITED KINGDOM reported OXCARBAZEPINE problem on Feb 28, 2008. Female patient, 42 years of age, weighting 141.1 lb, was diagnosed with epilepsy, psychotic disorder and was treated with OXCARBAZEPINE. After drug was administered, patient experienced the following problems/side effects: feeding disorder, gait disturbance, somnolence, . OXCARBAZEPINE dosage: 600 MG, BID. During the same period patient was treated with AMISULPRIDE, CLOBAZAM, LEVETIRACETAM, TEGRETOL. Patient recovered.

Synagis Side Effects Report #5683437-2
SYNAGIS problem was reported by a Physician from KOREA, REPUBLIC OF on Mar 17, 2008. Female patient, weighting 3.78 lb, was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: feeding disorder, . SYNAGIS dosage: 26 MG : 40 MG : 60 MG : 70 MG : 75 MG. During the same period patient was treated with THEOPHYLLINE, FERRIC HYDROXIDE POLYMALTOSE. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5602412-7
Physician from UNITED STATES reported SYNAGIS problem on Jan 10, 2008. Female patient was diagnosed with de lange's syndrome, foetal growth retardation, premature baby and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: feeding disorder, haemophilus infection, lethargy, moraxella infection, pallor, pneumonia respiratory syncytial viral, respiratory failure, upper respiratory tract infection, . SYNAGIS dosage: 55 MG, 1 IN 1 M, INTRAMUSCULAR; 50 MG, 1 IN 1 M, INTRAMUSCULAR; 50 MG, 1 IN 1 M, INTRAMUSCULAR. Patient was hospitalized. Patient recovered.

Topiramate Side Effects Report #5535961-0
TOPIRAMATE problem was reported by a Physician from UNITED STATES on Nov 29, 2007. Male patient, weighting 20.00 lb, was diagnosed with epilepsy and was treated with TOPIRAMATE. After drug was administered, patient experienced the following problems/side effects: feeding disorder, . TOPIRAMATE dosage: unknown. Patient was hospitalized. Patient recovered.


Triflucan Side Effects Report #5488774-2
Consumer or non-health professional from FRANCE reported TRIFLUCAN problem on Oct 05, 2007. Female patient, weighting 161.4 lb, was diagnosed with fungal infection and was treated with TRIFLUCAN. After drug was administered, patient experienced the following problems/side effects: feeding disorder, furuncle, genital discharge, hepatitis, hypertension, pain, skin disorder, type 2 diabetes mellitus, . TRIFLUCAN dosage: DAILY DOSE:50MG. During the same period patient was treated with XANAX, ZOLPIDEM TARTRATE. Patient recovered.

Triflucan Side Effects Report #5493954-6
TRIFLUCAN problem was reported by a Consumer or non-health professional from on Oct 11, 2007. Female patient, weighting 161.4 lb, was diagnosed with fungal infection and was treated with TRIFLUCAN. After drug was administered, patient experienced the following problems/side effects: feeding disorder, furuncle, genital discharge, hepatitis, hypertension, pain, skin disorder, type 2 diabetes mellitus, . TRIFLUCAN dosage: DAILY DOSE:50MG. During the same period patient was treated with XANAX, ZOLPIDEM TARTRATE. Patient recovered.

Cisplatin Side Effects Report #5382670-7
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on July 03, 2007. Male patient, weighting 172.0 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: feeding disorder, ill-defined disorder, nausea, vomiting, . CISPLATIN dosage: 188 MG. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5393810-8
BEVACIZUMAB problem was reported by a Health Professional from UNITED STATES on July 20, 2007. Male patient, weighting 201.3 lb, was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: feeding disorder, nausea, oral intake reduced, vomiting, weight decreased, . BEVACIZUMAB dosage: 5MG/KG Q 3 WEEKS IV. During the same period patient was treated with CISPLATIN. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5382670-7
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on July 03, 2007. Male patient, weighting 172.0 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: feeding disorder, ill-defined disorder, nausea, vomiting, . CISPLATIN dosage: 188 MG. Patient was hospitalized. Patient recovered.


Bevacizumab Side Effects Report #5393810-8
BEVACIZUMAB problem was reported by a Health Professional from UNITED STATES on July 20, 2007. Male patient, weighting 201.3 lb, was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: feeding disorder, nausea, oral intake reduced, vomiting, weight decreased, . BEVACIZUMAB dosage: 5MG/KG Q 3 WEEKS IV. During the same period patient was treated with CISPLATIN. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5705972-0
Physician from KOREA, REPUBLIC OF reported SYNAGIS problem on Mar 27, 2008. Female patient, weighting 3.78 lb, was diagnosed with antiviral prophylaxis and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: feeding disorder, . SYNAGIS dosage: 26 MG; 40 MG; 60 MG; 70 MG; 75 MG. During the same period patient was treated with THEOPHYLLINE, FERRIC HYDROXIDE POLYMALTOSE. Patient was hospitalized. Patient recovered.

Amifostine Side Effects Report #5724841-3
AMIFOSTINE problem was reported by a Pharmacist from UNITED STATES on Apr 30, 2008. Male patient, 59 years of age, was treated with AMIFOSTINE. After drug was administered, patient experienced the following problems/side effects: feeding disorder, haematemesis, nausea, . AMIFOSTINE dosage: 50 MG EVERY DAY IV. During the same period patient was treated with CETUXIMAB. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5367219-7
Physician from FRANCE reported ZOMETA problem on June 14, 2007. Female patient, weighting 149.9 lb, was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: feeding disorder, gingival pain, periodontal disease, tooth loss, toothache, weight decreased, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with NAVELBINE. Patient recovered.

Synagis Side Effects Report #5324454-1
SYNAGIS problem was reported by a Physician from FRANCE on Apr 23, 2007. Female patient, weighting 12.35 lb, was diagnosed with antiviral prophylaxis and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: feeding disorder, food intolerance, . SYNAGIS dosage: unknown. Patient was hospitalized. Patient recovered.


Synagis Side Effects Report #5334957-1
Physician from FRANCE reported SYNAGIS problem on May 09, 2007. Female patient, weighting 6.90 lb, was diagnosed with antiviral prophylaxis and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: feeding disorder, . SYNAGIS dosage: unknown. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5336623-5
SYNAGIS problem was reported by a Physician from FRANCE on May 10, 2007. Female patient was diagnosed with antiviral prophylaxis and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: feeding disorder, ileus, intestinal obstruction, sepsis, staphylococcal infection, viral infection, . SYNAGIS dosage: unknown. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5308204-0
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Apr 13, 2007. Male patient, 45 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: feeding disorder, implantable defibrillator insertion, myocardial infarction, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Topamax Side Effects Report #5274280-7
TOPAMAX problem was reported by a Health Professional from UNITED KINGDOM on Mar 12, 2007. Male patient, 47 years of age, was diagnosed with epilepsy and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: feeding disorder, speech disorder, weight decreased, . TOPAMAX dosage: unknown. During the same period patient was treated with VALPROATE, LAMOTRIGINE. Patient recovered.

Rapamune Side Effects Report #5643153-X
Health Professional from FRANCE reported RAPAMUNE problem on Feb 22, 2008. Male patient, child 10 years of age, was diagnosed with lymphoma and was treated with RAPAMUNE. After drug was administered, patient experienced the following problems/side effects: cheilitis, feeding disorder, gingival bleeding, gingival pain, weight decreased, . RAPAMUNE dosage: PROGRESSIVELY INCREASED UP TO 2 MG DAILY. Patient recovered.


Triflucan Side Effects Report #5511662-X
TRIFLUCAN problem was reported by a Consumer or non-health professional from FRANCE on Oct 30, 2007. Female patient, weighting 161.4 lb, was diagnosed with fungal infection and was treated with TRIFLUCAN. After drug was administered, patient experienced the following problems/side effects: blood triglycerides increased, feeding disorder, furuncle, genital discharge, hepatitis, hypertension, nail disorder, pain, skin disorder, . TRIFLUCAN dosage: DAILY DOSE:50MG. During the same period patient was treated with XANAX, STILNOX. Patient recovered.

Xeloda Side Effects Report #5404205-2
Consumer or non-health professional from UNITED STATES reported XELODA problem on July 24, 2007. Female patient was treated with XELODA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, feeding disorder, hepatic neoplasm, lung neoplasm, malaise, . XELODA dosage: DOSING SCHEDULE REPORTED AS 3 (500MG) TABS BID.. During the same period patient was treated with COMPAZINE, PRILOSEC, OXYCONTIN, NEURONTIN, FASLODEX, ZOMETA. Patient recovered.

Keppra Side Effects Report #5420702-8
KEPPRA problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Aug 02, 2007. Female patient, 40 years of age, was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: alopecia, feeding disorder, haemorrhage, platelet count decreased, tremor, weight decreased, . KEPPRA dosage: 750 MG / D. During the same period patient was treated with EPILIM. Patient recovered.

Baclofen Side Effects Report #5429592-0
Consumer or non-health professional from UNITED STATES reported BACLOFEN problem on Aug 09, 2007. Male patient, child 5 years of age, was diagnosed with muscle spasticity and was treated with BACLOFEN. After drug was administered, patient experienced the following problems/side effects: cerebral ventriculogram abnormal, feeding disorder, shunt malfunction, shunt occlusion, . BACLOFEN dosage: unknown. Patient recovered.

Cardioaspirin Side Effects Report #5389985-7
CARDIOASPIRIN problem was reported by a Physician from ITALY on July 10, 2007. Female patient, 76 years of age, was diagnosed with leukoencephalopathy and was treated with CARDIOASPIRIN. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, feeding disorder, . CARDIOASPIRIN dosage: TOTAL DAILY DOSE: 100 MG UNIT DOSE: 100 MG. Patient was hospitalized. Patient recovered.

Cardioaspirin Side Effects Report #5389985-7
Physician from ITALY reported CARDIOASPIRIN problem on July 10, 2007. Female patient, 76 years of age, was diagnosed with leukoencephalopathy and was treated with CARDIOASPIRIN. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, feeding disorder, . CARDIOASPIRIN dosage: TOTAL DAILY DOSE: 100 MG UNIT DOSE: 100 MG. Patient was hospitalized. Patient recovered.

Zosyn Side Effects Report #5743495-3
ZOSYN problem was reported by a Consumer or non-health professional from UNITED STATES on May 15, 2008. Female patient, weighting 125.1 lb, was diagnosed with pyrexia and was treated with ZOSYN. After drug was administered, patient experienced the following problems/side effects: diarrhoea, feeding disorder, haematochezia, pneumonia, . ZOSYN dosage: unknown. Patient was hospitalized. Patient recovered.

Ibritumomab Side Effects Report #5366252-9
Physician from UNITED STATES reported IBRITUMOMAB TIUXETAN problem on June 19, 2007. Female patient, weighting 126.0 lb, was treated with IBRITUMOMAB TIUXETAN. After drug was administered, patient experienced the following problems/side effects: breast cancer female, feeding disorder, gastric ulcer, impaired healing, malignant neoplasm progression, nausea, pain, vomiting, . IBRITUMOMAB TIUXETAN dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.

Erlotinib Side Effects Report #5371423-1
ERLOTINIB problem was reported by a Health Professional from UNITED STATES on June 07, 2007. Female patient, 55 years of age, weighting 158.1 lb, was diagnosed with squamous cell carcinoma and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: dysphagia, feeding disorder, hypertension, oral discomfort, pyrexia, . ERLOTINIB dosage: 150 MG (QD), ORAL. During the same period patient was treated with BEVACIZUMAB, CARBOPLATIN, PACLITAXEL, FLUOROURACIL, RADIATION. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5320870-2
Physician from FRANCE reported VELCADE problem on Apr 24, 2007. Male patient, 40 years of age, weighting 176.4 lb, was diagnosed with t-cell lymphoma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: febrile neutropenia, feeding disorder, mucosal inflammation, . VELCADE dosage: 3.00 MG, INTRAVENOUS. During the same period patient was treated with DOXORUBICIN, CYCLOPHOSPHAMIDE, ELDISINE, BLEOMYCIN, PREDNISONE, GRANOCYTE, BACTRIM, VALACYCLOVIR. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5304616-X
SYNAGIS problem was reported by a Physician from FRANCE on Apr 03, 2007. Female patient, weighting 6.79 lb, was diagnosed with bronchopulmonary dysplasia, premature baby and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: anorexia, feeding disorder, gastroenteritis, gastrooesophageal reflux disease, . SYNAGIS dosage: 75 MG, 1 IN 30 D, INTRAMUSCULAR. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5313584-6
Physician from FRANCE reported SYNAGIS problem on Apr 10, 2007. Female patient, weighting 11.02 lb, was diagnosed with antiviral prophylaxis and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: bronchiolitis, feeding disorder, . SYNAGIS dosage: unknown. Patient was hospitalized. Patient recovered.

Triflucan Side Effects Report #5605285-1
TRIFLUCAN problem was reported by a Consumer or non-health professional from FRANCE on Jan 17, 2008. Female patient, weighting 161.4 lb, was diagnosed with fungal infection and was treated with TRIFLUCAN. After drug was administered, patient experienced the following problems/side effects: dyspepsia, fatigue, feeding disorder, furuncle, genital discharge, hepatitis, hypertension, nail disorder, . TRIFLUCAN dosage: DAILY DOSE:50MG. During the same period patient was treated with XANAX, STILNOX. Patient recovered.

Velcade Side Effects Report #5494324-7
Consumer or non-health professional from FRANCE reported VELCADE problem on Oct 11, 2007. Female patient, 64 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: anaemia, bicytopenia, feeding disorder, hypokalaemia, inflammation, leukopenia, nausea, stomatitis, thrombocytopenia, . VELCADE dosage: 2.10 MG, INTRAVENOUS. During the same period patient was treated with DOXORUBICIN, DEXAMETHASONE. Patient was hospitalized. Patient recovered.

Lioresal Side Effects Report #5428950-8
LIORESAL problem was reported by a Physician from UNITED STATES on Aug 17, 2007. Male patient, child 5 years of age, was diagnosed with muscle spasticity and was treated with LIORESAL. After drug was administered, patient experienced the following problems/side effects: cerebral ventricle dilatation, device interaction, feeding disorder, food intolerance, ventriculoperitoneal shunt malfunction, . LIORESAL dosage: unknown. Patient recovered.

Erlotinib Side Effects Report #5764153-5
Physician from UNITED STATES reported ERLOTINIB problem on May 20, 2008. Female patient, 55 years of age, weighting 153.0 lb, was diagnosed with head and neck cancer and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: anaemia, cellulitis, feeding disorder, food intolerance, hypomagnesaemia, nausea, oral pain, vomiting, . ERLOTINIB dosage: (150 MG, QD) ORAL. During the same period patient was treated with CISPLATIN, SYMBAX, AMBIEN, ATIVAN, ROXICET, GLUCOVANCE, DILAUDID, FENTANYL. Patient was hospitalized. Patient recovered.

Neurontin Side Effects Report #5736708-5
NEURONTIN problem was reported by a Consumer or non-health professional from UNITED STATES on May 01, 2008. Female patient was diagnosed with epilepsy and was treated with NEURONTIN. After drug was administered, patient experienced the following problems/side effects: cleft palate, feeding disorder, . NEURONTIN dosage: DAILY DOSE:1200MG. During the same period patient was treated with TEGRETOL, SYNTHROID. Patient recovered.

Velcade Side Effects Report #5746193-5
Physician from FRANCE reported VELCADE problem on May 06, 2008. Female patient, 56 years of age, weighting 103.6 lb, was diagnosed with t-cell lymphoma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: aphthous stomatitis, febrile bone marrow aplasia, feeding disorder, odynophagia, oesophageal candidiasis, oral candidiasis, thrombocytopenia, . VELCADE dosage: unknown. During the same period patient was treated with DOXORUBICIN, CYCLOPHOSPHAMIDE, ELDISINE, BLEOMYCIN SULPHATE, METHOTREXATE, PREDNISONE, GRANOCYTE. Patient was hospitalized. Patient recovered.

Diovan Side Effects Report #5754078-3
DIOVAN problem was reported by a Consumer or non-health professional from BRAZIL on May 23, 2008. Male patient, 79 years of age, weighting 132.3 lb, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: arterial occlusive disease, asthenia, feeding disorder, gastrectomy, gastric cancer, . DIOVAN dosage: unknown. During the same period patient was treated with RENITEC, LIPITOR. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5334958-3
Physician from FRANCE reported SYNAGIS problem on May 09, 2007. Female patient, weighting 7.65 lb, was diagnosed with antiviral prophylaxis and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: bronchiolitis, bronchopulmonary dysplasia, feeding disorder, gastrooesophageal reflux disease, infantile asthma, . SYNAGIS dosage: unknown. Patient was hospitalized. Patient recovered.

Synagis Side Effects Report #5306563-6
SYNAGIS problem was reported by a Physician from FRANCE on Apr 03, 2007. Female patient, weighting 10.76 lb, was diagnosed with antiviral prophylaxis, bronchopulmonary dysplasia, premature baby and was treated with SYNAGIS. After drug was administered, patient experienced the following problems/side effects: anorexia, bronchiolitis, feeding disorder, gastroenteritis, . SYNAGIS dosage: 75 MG, 1 IN 30 D, INTRAMUSCULAR. During the same period patient was treated with VITAMIN D. Patient was hospitalized. Patient recovered.

Zometa Side Effects Report #5262524-7
Physician from FRANCE reported ZOMETA problem on Mar 07, 2007. Male patient, 66 years of age, weighting 136.7 lb, was diagnosed with metastases to bone, prostate cancer metastatic and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: condition aggravated, feeding disorder, fistula, gingival ulceration, ischaemic cardiomyopathy, jaw operation, osteitis, osteonecrosis, . ZOMETA dosage: 4 MG EVERY THREE WEEKS. During the same period patient was treated with NOVANTRONE, TAXOTERE, ESTRACYT, DIURETICS, ANDROCUR, ZOLADEX. Patient was hospitalized and became disabled. Patient died on 10/01/2006.