Menu

• Ask a Health Expert about GASTROINTESTINAL MOTILITY DISORDER
• Post Your Side Effect related to GASTROINTESTINAL MOTILITY DISORDER
• GASTROINTESTINAL MOTILITY DISORDER and FDA Warnings
• GASTROINTESTINAL MOTILITY DISORDER in Patients Wiki
• Report GASTROINTESTINAL MOTILITY DISORDER in Drug Side Effect Survey

GASTROINTESTINAL MOTILITY DISORDER side effect

What is GASTROINTESTINAL MOTILITY DISORDER ?

A Health Expert wants to answer your question. Please provide details below.

Type your question here

 letters left

Telzir Side Effects Report #5632102-6
Consumer or non-health professional from FRANCE reported TELZIR problem on Feb 18, 2008. Female patient, 37 years of age, was diagnosed with hiv infection and was treated with TELZIR. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, headache, hepatocellular injury, insomnia, lymphadenopathy, muscle spasms, myalgia, spontaneous haematoma, . TELZIR dosage: 700MG TWICE PER DAY. During the same period patient was treated with TRUVADA, NORVIR. Patient recovered.

Xusal Side Effects Report #5521659-1
XUSAL problem was reported by a Physician from GERMANY on Oct 30, 2007. Female patient, 19 years of age, weighting 110.2 lb, was treated with XUSAL. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, nausea, somnolence, suicide attempt, . XUSAL dosage: unknown. During the same period patient was treated with PARACETAMOL, ASPIRIN, PASPERTIN. Patient recovered.

Forteo Side Effects Report #5407375-5
Consumer or non-health professional from FRANCE reported FORTEO problem on July 30, 2007. Female patient, 74 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Reglan Side Effects Report #5420879-4
REGLAN problem was reported by a Physician from UNITED STATES on Aug 01, 2007. Female patient, 41 years of age, was treated with REGLAN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, nervous system disorder, . REGLAN dosage: unknown. Patient was hospitalized. Patient recovered.


Januvia Side Effects Report #5470400-X
Consumer or non-health professional from UNITED STATES reported JANUVIA problem on Apr 25, 2007. Male patient, 81 years of age, was diagnosed with diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, . JANUVIA dosage: 100 MG/DAILY/PO. During the same period patient was treated with AMARYL, DIOVAN. Patient recovered.

Avonex Side Effects Report #5387137-8
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on June 27, 2007. Female patient, 62 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, vomiting, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5387137-8
Consumer or non-health professional from UNITED STATES reported AVONEX problem on June 27, 2007. Female patient, 62 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, vomiting, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5737026-1
REMICADE problem was reported by a Physician from FRANCE on May 06, 2008. Male patient, 26 years of age, weighting 99.21 lb, was diagnosed with crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, intestinal stenosis, malnutrition, . REMICADE dosage: unknown. During the same period patient was treated with AZATHIAPRINE. Patient was hospitalized and became disabled. Patient recovered.

Nexium Side Effects Report #5370611-8
Consumer or non-health professional from NETHERLANDS reported NEXIUM problem on June 22, 2007. Male patient, weighting 202.8 lb, was diagnosed with gastrooesophageal reflux disease and was treated with NEXIUM. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, gynaecomastia, lymphadenopathy, . NEXIUM dosage: unknown. During the same period patient was treated with SUCRALFAAT SANDOZ SUSPENSIE. Patient recovered.


Infliximab Side Effects Report #5334271-4
INFLIXIMAB problem was reported by a Physician from FRANCE on May 15, 2007. Male patient, 26 years of age, weighting 99.21 lb, was diagnosed with crohn's disease and was treated with INFLIXIMAB. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, intestinal stenosis, malnutrition, . INFLIXIMAB dosage: unknown. During the same period patient was treated with AZATHIAPRINE. Patient was hospitalized and became disabled. Patient recovered.

Exjade Side Effects Report #5301808-0
Consumer or non-health professional from FRANCE reported EXJADE problem on Apr 05, 2007. Female patient, 72 years of age, was diagnosed with haemochromatosis and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, paraesthesia, . EXJADE dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, CHRONADALATE, DIAMICRON, COAPROVEL, RIVOTRIL, PARACETAMOL, ENDOTELON, RUBOZINC. Patient recovered.

Duragesic Side Effects Report #5310978-X
DURAGESIC problem was reported by a Health Professional from UNITED STATES on Apr 18, 2007. Female patient, weighting 264.0 lb, was diagnosed with breakthrough pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, . DURAGESIC dosage: unknown. During the same period patient was treated with LORTAB, MORPHINE, FENTANYL CITRATE, ZOLPIDEM TARTRATE, TIAGABINE, LEVOTHYROXINE, MONTELUKAST, TRIAMCINOLONE ACETONIDE. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5678757-1
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Mar 11, 2008. Female patient, 53 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: biliary tract disorder, gastrointestinal motility disorder, hypertrophy, intestinal obstruction, pancreatic disorder, procedural complication, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5629701-4
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 04, 2008. Male patient, 68 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: colon cancer, gastrointestinal motility disorder, micturition disorder, pain, pneumonia, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.


Lithium Side Effects Report #5632915-0
Consumer or non-health professional from SPAIN reported LITHIUM problem on Feb 04, 2008. Female patient, 32 years of age, was diagnosed with intentional overdose and was treated with LITHIUM. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, haemodialysis, intentional overdose, renal impairment, therapeutic agent toxicity, white blood cell count increased, . LITHIUM dosage: unknown. During the same period patient was treated with AMITRIPTYLINE, CLORAZEPATE, CLOMIPRAMINE, LORAZEPAM. Patient was hospitalized. Patient recovered.

Abilify Side Effects Report #5587991-0
ABILIFY problem was reported by a Physician from UNITED STATES on Jan 09, 2008. Male patient, 56 years of age, weighting 160.0 lb, was diagnosed with depression and was treated with ABILIFY. After drug was administered, patient experienced the following problems/side effects: akathisia, gastrointestinal motility disorder, respiratory dyskinesia, tardive dyskinesia, . ABILIFY dosage: 2.5 MG EVERY OTHER DAY ORAL. Patient recovered.

Rabeprazole Side Effects Report #5580016-2
Physician from JAPAN reported RABEPRAZOLE problem on Dec 17, 2007. Female patient, 68 years of age, was diagnosed with gastric ulcer and was treated with RABEPRAZOLE. After drug was administered, patient experienced the following problems/side effects: dizziness, gastrointestinal motility disorder, paralysis, vision blurred, . RABEPRAZOLE dosage: 10 MG, 1 IN 1 D, ORAL. During the same period patient was treated with ZETIA, OLMETEC, ANSATUR. Patient recovered.

Avonex Side Effects Report #5490013-3
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 04, 2007. Female patient, 68 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: colon cancer, gastrointestinal motility disorder, micturition disorder, pain, pneumonia, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Subutex Side Effects Report #5496637-1
Health Professional from FRANCE reported SUBUTEX problem on Oct 19, 2007. Male patient, 35 years of age, was treated with SUBUTEX. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, gastrointestinal motility disorder, vomiting, . SUBUTEX dosage: unknown. Patient was hospitalized. Patient died.


Subutex Side Effects Report #5501734-8
SUBUTEX problem was reported by a Health Professional from FRANCE on Oct 29, 2007. Male patient, 35 years of age, was treated with SUBUTEX. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, gastrointestinal motility disorder, vomiting, . SUBUTEX dosage: unknown. Patient was hospitalized. Patient died.

Subutex Side Effects Report #5503264-6
Health Professional from FRANCE reported SUBUTEX problem on Oct 29, 2007. Male patient, 35 years of age, was treated with SUBUTEX. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, gastrointestinal motility disorder, vomiting, . SUBUTEX dosage: unknown. Patient was hospitalized. Patient died.

Taxotere Side Effects Report #5403845-4
TAXOTERE problem was reported by a Physician from SWEDEN on July 27, 2007. Female patient was treated with TAXOTERE. After drug was administered, patient experienced the following problems/side effects: abasia, gastrointestinal motility disorder, nervous system disorder, urinary retention, . TAXOTERE dosage: unknown. During the same period patient was treated with HERCEPTIN. Patient recovered.

Byetta Side Effects Report #5773499-6
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Mar 12, 2008. Male patient, 59 years of age, weighting 224.9 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: decreased appetite, gastrointestinal motility disorder, nausea, vomiting, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with GLIMEPIRIDE, GLUCOPHAGE, AVANDIA. Patient recovered.

Avonex Side Effects Report #5722921-X
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 17, 2008. Female patient, 53 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: gastric mucosal hypertrophy, gastrointestinal motility disorder, nausea, pain, post procedural complication, postoperative adhesion, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Champix Side Effects Report #5357746-0
Health Professional from UNITED KINGDOM reported CHAMPIX problem on June 04, 2007. Female patient, 52 years of age, weighting 127.9 lb, was diagnosed with essential hypertension and was treated with CHAMPIX. After drug was administered, patient experienced the following problems/side effects: gastrointestinal motility disorder, joint swelling, liver function test abnormal, pain, renal impairment, . CHAMPIX dosage: unknown. During the same period patient was treated with AMLODIPINE. Patient recovered.

Zelnorm Side Effects Report #5313316-1
ZELNORM problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 26, 2007. Female patient was diagnosed with irritable bowel syndrome, gastrooesophageal reflux disease, anxiety, pain and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, gastrointestinal motility disorder, . ZELNORM dosage: 6 MG, BID. During the same period patient was treated with NEXIUM, ALPRAZOLAM, TYLENOL, VITAMIN CAP. Patient was hospitalized. Patient recovered.

Zelnorm Side Effects Report #5317479-3
Consumer or non-health professional from UNITED STATES reported ZELNORM problem on Apr 25, 2007. Female patient was diagnosed with irritable bowel syndrome, gastrooesophageal reflux disease, anxiety, pain and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, gastrointestinal motility disorder, . ZELNORM dosage: 6 MG, BID. During the same period patient was treated with NEXIUM, ALPRAZOLAM, TYLENOL, VITAMIN CAP. Patient was hospitalized. Patient recovered.

Remicade Side Effects Report #5329930-3
REMICADE problem was reported by a Physician from FRANCE on May 10, 2007. Male patient, 26 years of age, weighting 154.3 lb, was diagnosed with crohn's disease and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: colon cancer, gastrointestinal motility disorder, . REMICADE dosage: unknown. During the same period patient was treated with AZATHIOPRINE. Patient recovered.

Zelnorm Side Effects Report #5304147-7
Consumer or non-health professional from UNITED STATES reported ZELNORM problem on Apr 12, 2007. Female patient was diagnosed with irritable bowel syndrome, anxiety and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, gastrointestinal motility disorder, . ZELNORM dosage: 6 MG, BID. During the same period patient was treated with NEXIUM, ALPRAZOLAM. Patient was hospitalized. Patient recovered.

Venlafaxine Side Effects Report #5256945-6
VENLAFAXINE problem was reported by a Health Professional from GERMANY on Mar 02, 2007. Female patient, weighting 154.3 lb, was treated with VENLAFAXINE. After drug was administered, patient experienced the following problems/side effects: fatigue, gastrointestinal motility disorder, intentional overdose, . VENLAFAXINE dosage: OVERDOSE AMOUNT 2250 MG. During the same period patient was treated with TRIMIPRAMINE MALEATE, NOCTAMID, ACETYLSALICYLIC ACID SRT, RISPERDAL. Patient was hospitalized. Patient recovered.

Renagel Side Effects Report #5285492-0
Physician from UNITED STATES reported RENAGEL problem on Mar 14, 2007. Male patient, 53 years of age, was diagnosed with hyperphosphataemia and was treated with RENAGEL. After drug was administered, patient experienced the following problems/side effects: bezoar, gastrointestinal motility disorder, . RENAGEL dosage: unknown. Patient was hospitalized. Patient recovered.

Methotrexate Side Effects Report #5683233-6
METHOTREXATE problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 20, 2008. Female patient, weighting 160.0 lb, was diagnosed with prostatic specific antigen, rheumatoid arthritis and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: back pain, condition aggravated, gastrointestinal motility disorder, hypoaesthesia, osteoarthritis, paraesthesia, paralysis, psoriasis, spinal cord oedema, . METHOTREXATE dosage: unknown. During the same period patient was treated with HUMIRA, VICODIN, ALPRAZOLAM, CITALOPRAM HYDROBROMIDE, ESOMEPRAZOLE. Patient was hospitalized. Patient recovered.

Trental Side Effects Report #5633132-0
Consumer or non-health professional from UNITED STATES reported TRENTAL problem on Feb 14, 2008. Female patient, weighting 130.1 lb, was treated with TRENTAL. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, asthenia, gastrointestinal motility disorder, hypokinesia, influenza like illness, loss of consciousness, vomiting, weight decreased, . TRENTAL dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, ASPIRIN, TRICOR, SPIRONOLACTONE, HYDROCHLOROTHIAZIDE, ATENOLOL, FOLIC ACID. Patient recovered.

Trental Side Effects Report #5601489-2
TRENTAL problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 17, 2008. Female patient, weighting 130.1 lb, was treated with TRENTAL. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, asthenia, gastrointestinal motility disorder, hypokinesia, influenza like illness, loss of consciousness, vomiting, weight decreased, . TRENTAL dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, ASPIRIN, TRICOR, SPIRONOLACTONE, HYDROCHLOROTHIAZIDE, ATENOLOL, FOLIC ACID. Patient recovered.

Lamivudine Side Effects Report #5481420-3
Consumer or non-health professional from UNITED STATES reported LAMIVUDINE problem on Oct 04, 2007. Male patient, 24 years of age, was treated with LAMIVUDINE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, gastritis, gastrointestinal motility disorder, hepatomegaly, nausea, vomiting, weight decreased, . LAMIVUDINE dosage: unknown. During the same period patient was treated with BACTRIM, ETHAMBUTOL, ZITHROMAX, REYATAZ, VIDEX, KALETRA. Patient recovered.

Zithromax Side Effects Report #5486120-1
ZITHROMAX problem was reported by a Health Professional from UNITED STATES on Oct 03, 2007. Male patient, 24 years of age, was treated with ZITHROMAX. After drug was administered, patient experienced the following problems/side effects: abdominal pain, gastritis, gastrointestinal motility disorder, hepatomegaly, nausea, vomiting, weight decreased, . ZITHROMAX dosage: DAILY DOSE:600MG. During the same period patient was treated with ETIBI, REYATAZ, VIDEX, LAMIVUDINE, VIREAD, KALETRA, BACTRIM. Patient recovered.

Viread Side Effects Report #5495404-2
Consumer or non-health professional from UNITED STATES reported VIREAD problem on Oct 15, 2007. Male patient, 24 years of age, was treated with VIREAD. After drug was administered, patient experienced the following problems/side effects: abdominal pain, gastritis, gastrointestinal motility disorder, hepatomegaly, nausea, vomiting, weight decreased, . VIREAD dosage: unknown. During the same period patient was treated with ETIBI, ZITHROMAX, REYATAZ, VIDEX, LAMIVUDINE, KALETRA, BACTRIM. Patient recovered.

Neurontin Side Effects Report #5497873-0
NEURONTIN problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 01, 2006. Female patient, 80 years of age, was diagnosed with neuropathy peripheral and was treated with NEURONTIN. After drug was administered, patient experienced the following problems/side effects: dizziness, fatigue, gastrointestinal motility disorder, ill-defined disorder, pain, tremor, vision blurred, . NEURONTIN dosage: 600 MG (300 MG, 2 IN 1 D). During the same period patient was treated with LYRICA, FOSAMAX, FEMHRT, CORTISONE ACETATE. Patient recovered.

Effexor Side Effects Report #5448573-4
Physician from SWITZERLAND reported EFFEXOR problem on Sept 05, 2007. Female patient, 41 years of age, was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, constipation, gastrointestinal motility disorder, nausea, . EFFEXOR dosage: unknown. During the same period patient was treated with SEROQUEL, ZURCAL, FERRUM HAUSMANN. Patient was hospitalized. Patient recovered.

Pegasys Side Effects Report #5469595-3
PEGASYS problem was reported by a Consumer or non-health professional from NORWAY on Aug 22, 2007. Female patient, 47 years of age, was diagnosed with pain and was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: asthenia, cold sweat, gastrointestinal motility disorder, heart rate increased, malaise, muscle twitching, myalgia, nervousness, palpitations, . PEGASYS dosage: unknown. During the same period patient was treated with COPEGUS, PARALGINTE, TRAMAGETIC, DURAGESIC. Patient recovered.

Januvia Side Effects Report #5469012-3
Consumer or non-health professional from UNITED STATES reported JANUVIA problem on June 19, 2007. Female patient, 69 years of age, was diagnosed with diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, dysgeusia, gastrointestinal motility disorder, vomiting, . JANUVIA dosage: 100 MG/DAILY/PO. During the same period patient was treated with MICARDIS, ZOCOR, ASPIRIN, INSULIN. Patient recovered.

Fosrenol Side Effects Report #5744910-1
FOSRENOL problem was reported by a Physician from ITALY on May 08, 2008. Male patient, 50 years of age, was diagnosed with hyperphosphataemia and was treated with FOSRENOL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, constipation, gastrointestinal motility disorder, peritoneal adhesions, x-ray abnormal, . FOSRENOL dosage: unknown. Patient was hospitalized. Patient recovered.

Effexor Side Effects Report #5344119-X
Physician from SWITZERLAND reported EFFEXOR problem on May 24, 2007. Female patient, 41 years of age, was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, constipation, gastrointestinal motility disorder, nausea, . EFFEXOR dosage: unknown. During the same period patient was treated with SEROQUEL, PANTOPRAZOLE, FERRUM HAUSMANN. Patient was hospitalized. Patient recovered.

Lortab Side Effects Report #5321165-3
LORTAB problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 19, 2007. Female patient, 36 years of age, weighting 264.6 lb, was diagnosed with breakthrough pain and was treated with LORTAB. After drug was administered, patient experienced the following problems/side effects: abdominal pain, constipation, gastrointestinal motility disorder, . LORTAB dosage: unknown. During the same period patient was treated with FENTANYL, MORPHINE, DURAGESIC, ZOLPIDEM TARTRATE, TIAGABINE, LEVOTHYROXINE, MONTELUKAST, TRIAMCINOLONE ACETONIDE. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5301291-5
Physician from JAPAN reported PROGRAF problem on Mar 29, 2007. Male patient, weighting 163.1 lb, was diagnosed with dermatitis atopic and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: cell marker increased, chromosome abnormality, gastrointestinal motility disorder, non-hodgkin's lymphoma, . PROGRAF dosage: unknown. During the same period patient was treated with MYSER, KINDAVATE. Patient was hospitalized. Patient recovered.

Nexavar Side Effects Report #5212702-8
NEXAVAR problem was reported by a Physician from UNITED STATES on Aug 28, 2006. Female patient, 48 years of age, was treated with NEXAVAR. After drug was administered, patient experienced the following problems/side effects: abdominal pain, blood amylase increased, gastrointestinal motility disorder, nausea, pancreatitis, rash, subileus, vomiting, . NEXAVAR dosage: 400 MG, BID, ORAL. During the same period patient was treated with DURAGESIC, FLEXERIL, AMBIEN, PHENERGAN, NEOSPORIN EYE AND EAR. Patient was hospitalized. Patient recovered.

Xifaxan Side Effects Report #5281298-7
Consumer or non-health professional from UNITED STATES reported XIFAXAN problem on May 22, 2006. Male patient was diagnosed with diarrhoea and was treated with XIFAXAN. After drug was administered, patient experienced the following problems/side effects: flatulence, frequent bowel movements, gastrointestinal motility disorder, pyrexia, . XIFAXAN dosage: 200MG/TID, ORAL. Patient recovered.