BEZOAR side effect
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Drugs associated with BEZOAR
ACTIVATED ADALAT CALCIUM CARBAMAZEPINE CHOLESTYRAMINE CYCLOSPORINE DEPAKOTE IBUPROFEN LOTRONEX NIFEDIPINE NORVASC PRECOSE PROGRAF RENAGEL SOTAHEXAL SOTALOL THEOPHYLLINELotronex Side Effects Report #5611477-8
Consumer or non-health professional from UNITED STATES reported LOTRONEX problem on Aug 07, 2007. Female patient, 72 years of age, was diagnosed with irritable bowel syndrome and was treated with LOTRONEX. After drug was administered, patient experienced the following problems/side effects: bezoar, dysphasia, impaired gastric emptying, . LOTRONEX dosage: 1MG PER DAY. During the same period patient was treated with AMARYL, LANOXIN, COUMADIN, FOLIC ACID, GLUCOPHAGE, ALLOPURINOL, PREMARIN, HYZAAR. Patient recovered.
Precose Side Effects Report #5521695-5
PRECOSE problem was reported by a Pharmacist from UNITED STATES on Nov 08, 2007. Female patient, weighting 132.3 lb, was treated with PRECOSE. After drug was administered, patient experienced the following problems/side effects: bezoar, . PRECOSE dosage: TOTAL DAILY DOSE: 150 MG. During the same period patient was treated with GLYBURIDE. Patient recovered.
Precose Side Effects Report #5524575-4
Pharmacist from UNITED STATES reported PRECOSE problem on Nov 08, 2007. Female patient, weighting 132.3 lb, was treated with PRECOSE. After drug was administered, patient experienced the following problems/side effects: bezoar, . PRECOSE dosage: TOTAL DAILY DOSE: 150 MG. During the same period patient was treated with GLYBURIDE. Patient recovered.
Precose Side Effects Report #5480193-8
PRECOSE problem was reported by a Pharmacist from UNITED STATES on Oct 01, 2007. Female patient, weighting 132.3 lb, was treated with PRECOSE. After drug was administered, patient experienced the following problems/side effects: bezoar, . PRECOSE dosage: TOTAL DAILY DOSE: 150 MG. During the same period patient was treated with GLYBURIDE. Patient recovered.
Carbamazepine Side Effects Report #5455083-7
Consumer or non-health professional from ISRAEL reported CARBAMAZEPINE problem on Aug 20, 2007. Male patient, 25 years of age, was diagnosed with borderline personality disorder and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: bezoar, coma, convulsion, grand mal convulsion, hyponatraemia, pneumonia aspiration, pneumonia bacterial, sepsis, . CARBAMAZEPINE dosage: unknown. During the same period patient was treated with PAROXETINE, LITHIUM CARBONATE, RISPERIDONE. Patient recovered.
Ibuprofen Side Effects Report #5412962-4
IBUPROFEN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on July 26, 2007. Female patient, 54 years of age, was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: bezoar, cardiac arrest, lethargy, overdose, tachycardia, . IBUPROFEN dosage: unknown. During the same period patient was treated with THEOPHYLLINE, FORMED BEZOAR. Patient died.
Prograf Side Effects Report #5414599-X
Physician from UNITED STATES reported PROGRAF problem on July 31, 2007. Male patient, 47 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: bezoar, diarrhoea haemorrhagic, gastrointestinal disorder, gastrointestinal haemorrhage, impaired gastric emptying, vagus nerve disorder, . PROGRAF dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient was hospitalized. Patient recovered.
Ibuprofen Side Effects Report #5414947-0
IBUPROFEN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on July 26, 2007. Female patient, 54 years of age, was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: bezoar, cardiac arrest, lethargy, overdose, tachycardia, . IBUPROFEN dosage: unknown. During the same period patient was treated with THEOPHYLLINE. Patient died.
Theophylline Side Effects Report #5416747-4
Consumer or non-health professional from reported THEOPHYLLINE problem on Aug 06, 2007. Female patient, 54 years of age, was treated with THEOPHYLLINE. After drug was administered, patient experienced the following problems/side effects: bezoar, cardiac arrest, lethargy, overdose, tachycardia, vomiting, . THEOPHYLLINE dosage: unknown. During the same period patient was treated with IBUPROFEN, ISOSORBIDE DINITRATE, FUROSEMIDE, CONJUGATED OESTROGEN, DILTIAZEM HYDROCHLORIDE, DIGOXIN. Patient died.
Ibuprofen Side Effects Report #5423158-4
IBUPROFEN problem was reported by a Health Professional from UNITED KINGDOM on Aug 10, 2007. Female patient, 54 years of age, was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: bezoar, cardiac arrest, lethargy, tachycardia, . IBUPROFEN dosage: unknown. During the same period patient was treated with THEOPHYLLINE, FORMED. Patient died.
Prograf Side Effects Report #5424852-1
Physician from UNITED STATES reported PROGRAF problem on July 31, 2007. Female patient, 52 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: bezoar, disease recurrence, . PROGRAF dosage: unknown. Patient was hospitalized. Patient recovered.
Nifedipine Side Effects Report #5782956-8
NIFEDIPINE problem was reported by a Consumer or non-health professional from FRANCE on June 16, 2008. Female patient, 88 years of age, was diagnosed with hypertension and was treated with NIFEDIPINE. After drug was administered, patient experienced the following problems/side effects: bezoar, . NIFEDIPINE dosage: unknown. Patient was hospitalized. Patient recovered.
Nifedipine Side Effects Report #5752094-9
Consumer or non-health professional from FRANCE reported NIFEDIPINE problem on May 19, 2008. Female patient, 88 years of age, was diagnosed with hypertension and was treated with NIFEDIPINE. After drug was administered, patient experienced the following problems/side effects: bezoar, . NIFEDIPINE dosage: unknown. Patient was hospitalized. Patient recovered.
Nifedipine Side Effects Report #5694385-6
NIFEDIPINE problem was reported by a Consumer or non-health professional from FRANCE on Mar 27, 2008. Female patient, 88 years of age, was diagnosed with hypertension and was treated with NIFEDIPINE. After drug was administered, patient experienced the following problems/side effects: bezoar, colonic obstruction, faecal vomiting, flatulence, . NIFEDIPINE dosage: unknown. Patient was hospitalized. Patient recovered.
Sotahexal Side Effects Report #5336471-6
Physician from POLAND reported SOTAHEXAL problem on May 10, 2007. Female patient, 72 years of age, was diagnosed with palpitations and was treated with SOTAHEXAL. After drug was administered, patient experienced the following problems/side effects: bezoar, bile output, blood potassium increased, duodenogastric reflux, gastritis erosive, hypotension, . SOTAHEXAL dosage: 160 MG, ORAL. During the same period patient was treated with KALDYUM, RELANIUM. Patient recovered.
Depakote Side Effects Report #5275012-9
DEPAKOTE problem was reported by a Physician from UNITED STATES on Mar 16, 2007. Male patient, child 2 years of age, weighting 15.43 lb, was diagnosed with convulsion and was treated with DEPAKOTE. After drug was administered, patient experienced the following problems/side effects: bezoar, . DEPAKOTE dosage: 112 MG/KG. 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.
Carbamazepine Side Effects Report #5629802-0
CARBAMAZEPINE problem was reported by a Consumer or non-health professional from ISRAEL on Jan 31, 2008. Male patient, 25 years of age, was diagnosed with borderline personality disorder and was treated with CARBAMAZEPINE. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, bezoar, blood creatine phosphokinase increased, cardiovascular disorder, coma, faeces discoloured, gamma-glutamyltransferase increased, hypernatraemia, . CARBAMAZEPINE dosage: unknown. During the same period patient was treated with PAROXETINE, RISPERIDONE, LITHIUM CARBONATE. Patient was hospitalized. Patient recovered.
Calcium Side Effects Report #5631139-0
Consumer or non-health professional from reported CALCIUM CARBONATE problem on Feb 18, 2008. Female patient, 55 years of age, was treated with CALCIUM CARBONATE. After drug was administered, patient experienced the following problems/side effects: anorexia, bezoar, blood albumin decreased, hypotension, malnutrition, nausea, protein total decreased, vomiting, . CALCIUM CARBONATE dosage: unknown. During the same period patient was treated with ANTACID. Patient was hospitalized. Patient recovered.
Activated Side Effects Report #5731799-X
ACTIVATED CHARCOAL problem was reported by a Consumer or non-health professional from AUSTRALIA on Apr 24, 2008. Female patient, 30 years of age, was treated with ACTIVATED CHARCOAL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, bezoar, intestinal obstruction, nausea, overdose, somnolence, suicide attempt, urinary tract infection, . ACTIVATED CHARCOAL dosage: unknown. During the same period patient was treated with CARBAMAZEPINE, ALPRAZOLAM. Patient was hospitalized. Patient recovered.
Adalat Side Effects Report #5691393-6
Health Professional from FRANCE reported ADALAT problem on Mar 26, 2008. Female patient, 88 years of age, was diagnosed with hypertension and was treated with ADALAT. After drug was administered, patient experienced the following problems/side effects: abdominal distension, bezoar, faecal vomiting, intestinal obstruction, . ADALAT dosage: unknown. Patient was hospitalized. Patient recovered.
Sotalol Side Effects Report #5341391-7
SOTALOL problem was reported by a Physician from POLAND on May 15, 2007. Female patient, 72 years of age, was diagnosed with palpitations and was treated with SOTALOL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, bezoar, bile output, blood potassium increased, duodenogastric reflux, gastritis erosive, helicobacter pylori identification test positive, hypotension, malaise, . SOTALOL dosage: 160 MG, ORAL. During the same period patient was treated with KALDYUM, RELANIUM. Patient recovered.
Activated Side Effects Report #5343411-2
Consumer or non-health professional from UNITED STATES reported ACTIVATED CHARCOAL problem on May 16, 2007. Male patient, 21 years of age, was diagnosed with agitation, pain and was treated with ACTIVATED CHARCOAL. After drug was administered, patient experienced the following problems/side effects: agitation, bezoar, pain, small intestinal obstruction, . ACTIVATED CHARCOAL dosage: unknown. During the same period patient was treated with AMITRIPTLINE, MORPHINE, PHENYTOIN, DIAZEPAM, LIDOCAINE, NOREPINEPHRINE BITARTRATE. Patient was hospitalized. Patient recovered.
Cyclosporine Side Effects Report #5389822-0
CYCLOSPORINE problem was reported by a Health Professional from UNITED STATES on July 06, 2007. Male patient, 47 years of age, was diagnosed with lung transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: abdominal distension, abdominal pain, bezoar, diarrhoea haemorrhagic, gastrointestinal haemorrhage, impaired gastric emptying, therapeutic embolisation, . CYCLOSPORINE dosage: unknown. Patient was hospitalized. Patient recovered.
Norvasc Side Effects Report #5398204-7
Consumer or non-health professional from UNITED STATES reported NORVASC problem on July 16, 2007. Female patient, 50 years of age, was diagnosed with suicide attempt and was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, aspiration, bezoar, completed suicide, hypotension, intentional overdose, loss of consciousness, . NORVASC dosage: unknown. During the same period patient was treated with BENADRYL, AMITRIPTYLINE HYDROCHLORIDE. Patient was hospitalized. Patient died.
Cyclosporine Side Effects Report #5389822-0
CYCLOSPORINE problem was reported by a Health Professional from UNITED STATES on July 06, 2007. Male patient, 47 years of age, was diagnosed with lung transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: abdominal distension, abdominal pain, bezoar, diarrhoea haemorrhagic, gastrointestinal haemorrhage, impaired gastric emptying, therapeutic embolisation, . CYCLOSPORINE dosage: unknown. Patient was hospitalized. Patient recovered.
Norvasc Side Effects Report #5398204-7
Consumer or non-health professional from UNITED STATES reported NORVASC problem on July 16, 2007. Female patient, 50 years of age, was diagnosed with suicide attempt and was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, aspiration, bezoar, completed suicide, hypotension, intentional overdose, loss of consciousness, . NORVASC dosage: unknown. During the same period patient was treated with BENADRYL, AMITRIPTYLINE HYDROCHLORIDE. Patient was hospitalized. Patient died.
Cholestyramine Side Effects Report #5776669-6
CHOLESTYRAMINE problem was reported by a Health Professional from FRANCE on May 28, 2008. Female patient, 79 years of age, was diagnosed with prophylaxis, upper gastrointestinal haemorrhage and was treated with CHOLESTYRAMINE. After drug was administered, patient experienced the following problems/side effects: aspiration, aspiration tracheal, bezoar, flatulence, impaired gastric emptying, intestinal obstruction, respiratory distress, upper gastrointestinal haemorrhage, . CHOLESTYRAMINE dosage: unknown. During the same period patient was treated with OMEPRAZOLE, LACTULOSE. Patient was hospitalized. Patient recovered.
Cholestyramine Side Effects Report #5794556-4
Health Professional from FRANCE reported CHOLESTYRAMINE problem on June 17, 2008. Female patient, 79 years of age, was diagnosed with pruritus, prophylaxis, upper gastrointestinal haemorrhage and was treated with CHOLESTYRAMINE. After drug was administered, patient experienced the following problems/side effects: aspiration, aspiration tracheal, bezoar, intestinal obstruction, mechanical ventilation, respiratory distress, . CHOLESTYRAMINE dosage: unknown. During the same period patient was treated with OMEPRAZOLE, LACTULOSE. Patient was hospitalized. Patient recovered.