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GASTROINTESTINAL ULCER side effect

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Aleve Side Effects Report #5659832-4
Consumer or non-health professional from UNITED STATES reported ALEVE problem on Sept 14, 2007. Female patient, 67 years of age, weighting 200.6 lb, was diagnosed with arthritis, ischaemic heart disease prophylaxis and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, . ALEVE dosage: UNIT DOSE: 220 MG. During the same period patient was treated with ASPIRIN, OMEPRAZOLE, LASIX, DILTIAZEM, LEXAPRO, LISINOPRIL, SIMVASTATIN. Patient recovered.

Erlotinib Side Effects Report #5626152-3
ERLOTINIB problem was reported by a Physician from UNITED STATES on Feb 07, 2008. Female patient, 86 years of age, weighting 120.0 lb, was diagnosed with non-small cell lung cancer, coronary artery disease and was treated with ERLOTINIB. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, . ERLOTINIB dosage: 150 MG, QD. During the same period patient was treated with BEVACIZUMAB, ASPIRIN. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5535078-5
Consumer or non-health professional from AUSTRALIA reported ACTONEL problem on Nov 21, 2007. Female patient, 73 years of age, was diagnosed with osteoporosis and was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, rectal haemorrhage, . ACTONEL dosage: unknown. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5508140-0
BEVACIZUMAB problem was reported by a Physician from UNITED STATES on Oct 25, 2007. Male patient, weighting 162.0 lb, was diagnosed with colon cancer, hypertension, diabetes mellitus, hypercholesterolaemia and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, . BEVACIZUMAB dosage: 7.5 MG/KG, Q3W. During the same period patient was treated with XELODA, METOPROLOL, METFORMIN, LISINOPRIL, NIACIN, PLAVIX. Patient was hospitalized. Patient recovered.


Rituxan Side Effects Report #5526038-9
Consumer or non-health professional from UNITED STATES reported RITUXAN problem on Nov 20, 2007. Female patient was diagnosed with waldenstrom's macroglobulinaemia and was treated with RITUXAN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, irritable bowel syndrome, . RITUXAN dosage: unknown. Patient recovered.

Rituxan Side Effects Report #5499963-5
RITUXAN problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 18, 2007. Female patient was diagnosed with waldenstrom's macroglobulinaemia and was treated with RITUXAN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, irritable bowel syndrome, . RITUXAN dosage: unknown. Patient recovered.

Prednisolone Side Effects Report #5405610-0
Consumer or non-health professional from JAPAN reported PREDNISOLONE problem on July 30, 2007. Female patient, 67 years of age, was diagnosed with rheumatoid arthritis and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, haematochezia, ileal stenosis, . PREDNISOLONE dosage: unknown. During the same period patient was treated with MISOPROSTOL, DICLOFENAC. Patient was hospitalized. Patient recovered.

Prednisolone Side Effects Report #5411752-6
PREDNISOLONE problem was reported by a Consumer or non-health professional from JAPAN on Aug 06, 2007. Female patient, 67 years of age, was diagnosed with rheumatoid arthritis and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, haematochezia, ileal stenosis, . PREDNISOLONE dosage: unknown. During the same period patient was treated with MISOPROSTOL, VOLTAREN. Patient was hospitalized. Patient recovered.

Aspirin Side Effects Report #5721235-1
Health Professional from CANADA reported ASPIRIN problem on Apr 17, 2008. Male patient, 74 years of age, was diagnosed with arthralgia and was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, rectal haemorrhage, stomach discomfort, . ASPIRIN dosage: unknown. Patient recovered.


Alka Side Effects Report #5322100-4
ALKA SELTZER EFFERVESCENT PLUS COLD problem was reported by a Consumer or non-health professional from UNITED STATES on May 07, 2007. Female patient, 65 years of age, weighting 145.5 lb, was diagnosed with nasopharyngitis and was treated with ALKA SELTZER EFFERVESCENT PLUS COLD. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, rectal haemorrhage, . ALKA SELTZER EFFERVESCENT PLUS COLD dosage: unknown. During the same period patient was treated with ACTONEL, CELEBREX, LISINO HCTZ. Patient recovered.

Ibuprofen Side Effects Report #5333196-8
Consumer or non-health professional from UNITED STATES reported IBUPROFEN problem on May 21, 2007. Male patient, 63 years of age, was diagnosed with pain and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, . IBUPROFEN dosage: 800MG QID PO. Patient was hospitalized. Patient recovered.

Naproxen Side Effects Report #5349573-5
NAPROXEN problem was reported by a Physician from UNITED STATES on Dec 13, 2006. Female patient was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, . NAPROXEN dosage: 500 MG 2 PER DAY ORAL. Patient recovered.

Naproxen Side Effects Report #5349574-7
Physician from UNITED STATES reported NAPROXEN problem on Dec 13, 2006. Female patient was treated with NAPROXEN. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, . NAPROXEN dosage: 500 MG 2 PER DAY ORAL. Patient recovered.

Januvia Side Effects Report #5323211-X
JANUVIA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 11, 2007. Male patient, 64 years of age, was diagnosed with diabetes mellitus non-insulin-dependent and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, . JANUVIA dosage: 100 MG/DAILY/PO. Patient recovered.


Cetuximab Side Effects Report #5269511-3
Health Professional from UNITED STATES reported CETUXIMAB problem on Mar 15, 2007. Male patient, 55 years of age, was diagnosed with non-small cell lung cancer and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, haemoglobin decreased, malignant neoplasm progression, stress ulcer, . CETUXIMAB dosage: unknown. During the same period patient was treated with CARBOPLATIN, GEMCITABINE. Patient was hospitalized. Patient died on 11/23/2006.

Cetuximab Side Effects Report #5278779-9
CETUXIMAB problem was reported by a Health Professional from UNITED STATES on Mar 26, 2007. Male patient, 55 years of age, was diagnosed with non-small cell lung cancer and was treated with CETUXIMAB. After drug was administered, patient experienced the following problems/side effects: gastrointestinal ulcer, malignant neoplasm progression, . CETUXIMAB dosage: unknown. During the same period patient was treated with CARBOPLATIN, GEMCITABINE. Patient was hospitalized. Patient died on 11/23/2006.

Arixtra Side Effects Report #5684352-0
Physician from JAPAN reported ARIXTRA problem on Mar 27, 2008. Female patient, 79 years of age, weighting 134.5 lb, was diagnosed with thrombosis prophylaxis, hypertension, osteoarthritis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: dizziness, gastrointestinal ulcer, meniere's disease, nausea, vomiting, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with DIOVAN, BONALON, LORCAM. Patient was hospitalized. Patient recovered.

Warfarin Side Effects Report #5628606-2
WARFARIN problem was reported by a Pharmacist from UNITED STATES on Feb 14, 2008. Male patient, 77 years of age, weighting 174.2 lb, was diagnosed with deep vein thrombosis and was treated with WARFARIN. After drug was administered, patient experienced the following problems/side effects: gastric haemorrhage, gastrointestinal ulcer, international normalised ratio increased, . WARFARIN dosage: unknown. Patient was hospitalized. Patient recovered.

Bevacizumab Side Effects Report #5633781-X
Physician from UNITED KINGDOM reported BEVACIZUMAB problem on Feb 08, 2008. Male patient, weighting 165.3 lb, was diagnosed with non-small cell lung cancer and was treated with BEVACIZUMAB. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, gastrointestinal ulcer, . BEVACIZUMAB dosage: 15 MG/KG, Q3W. During the same period patient was treated with ASCAL, PERSANTINE, DEXAMETHASONE. Patient was hospitalized. Patient recovered.


Rituximab Side Effects Report #5579424-5
RITUXIMAB problem was reported by a Physician from GERMANY on Dec 21, 2007. Male patient, weighting 242.5 lb, was diagnosed with chronic lymphocytic leukaemia and was treated with RITUXIMAB. After drug was administered, patient experienced the following problems/side effects: dysphagia, gastrointestinal ulcer, . RITUXIMAB dosage: unknown. During the same period patient was treated with FLUDARABINE PHOSPHATE, CYCLOPHOSPHAMIDE, NORVASC, TRIAMTERENE AND HYDROCHLOROTHIAZIDE, NEUPOGEN, NEXIUM. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5490728-7
Physician from JAPAN reported ARIXTRA problem on Oct 12, 2007. Female patient, 42 years of age, weighting 123.5 lb, was diagnosed with thrombosis prophylaxis, application site pain and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, gastrointestinal ulcer, haemoglobin decreased, post procedural haematoma, subcutaneous haematoma, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with LORCAM, LIVALO, OLMETEC, THEOPHYLLINE, ZYLORIC, LORAZEPAM, DIGOXIN SEMI, MUCOSTA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5499397-3
ARIXTRA problem was reported by a Physician from JAPAN on Oct 24, 2007. Female patient, 42 years of age, weighting 123.5 lb, was diagnosed with thrombosis prophylaxis, application site pain and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage, gastrointestinal ulcer, haemoglobin decreased, post procedural haematoma, subcutaneous haematoma, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with LORCAM, LIVALO, OLMETEC, THEOPHYLLINE, ZYLORIC, LORAZEPAM, DIGOXIN SEMI, MUCOSTA. Patient was hospitalized. Patient recovered.

Aleve Side Effects Report #5771504-4
Consumer or non-health professional from UNITED STATES reported ALEVE problem on June 03, 2008. Female patient, 64 years of age, weighting 169.8 lb, was diagnosed with arthralgia and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: gastric ulcer, gastrointestinal ulcer, . ALEVE dosage: TOTAL DAILY DOSE: 880 MG UNIT DOSE: 220 MG. During the same period patient was treated with PLAQUENIL, SYNTHROID, CALCIUM, FISH OIL, GARLIC S, ZOVIRAX. Patient recovered.

Avonex Side Effects Report #5748206-3
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on May 07, 2008. Female patient, 56 years of age, weighting 90.00 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: constipation, gastrointestinal ulcer, influenza like illness, liver disorder, nasopharyngitis, oesophageal ulcer, pancreatic disorder, . AVONEX dosage: unknown. During the same period patient was treated with DURAGESIC. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5708154-1
Physician from JAPAN reported ARIXTRA problem on Apr 11, 2008. Female patient, 79 years of age, weighting 134.5 lb, was diagnosed with thrombosis prophylaxis, hypertension, osteoarthritis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: dizziness, gastrointestinal ulcer, meniere's disease, nausea, vomiting, . ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with DIOVAN, BONALON, LORCAM. Patient was hospitalized. Patient recovered.

Alka Side Effects Report #5358286-5
ALKA SELTZER EFFERVESCENT PLUS COLD problem was reported by a Consumer or non-health professional from UNITED STATES on June 11, 2007. Female patient, 65 years of age, weighting 149.9 lb, was diagnosed with nasopharyngitis and was treated with ALKA SELTZER EFFERVESCENT PLUS COLD. After drug was administered, patient experienced the following problems/side effects: colitis, gastrointestinal ulcer, rectal haemorrhage, . ALKA SELTZER EFFERVESCENT PLUS COLD dosage: TOTAL DAILY DOSE: 500 MG UNIT DOSE: 250 MG. During the same period patient was treated with ACTONEL, CELEBREX, LISINO HCTZ. Patient recovered.

Rebif Side Effects Report #5314569-6
Consumer or non-health professional from UNITED STATES reported REBIF problem on Apr 16, 2007. Male patient, 50 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: abdominal pain, gastrointestinal ulcer, weight decreased, . REBIF dosage: unknown. During the same period patient was treated with ASPIRIN. Patient was hospitalized. Patient recovered.

Aleve Side Effects Report #5338877-8
ALEVE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 18, 2006. Male patient, 76 years of age, weighting 275.0 lb, was diagnosed with pain and was treated with ALEVE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, gastrointestinal ulcer, ulcer haemorrhage, . ALEVE dosage: 220 MG, PRN, ORAL. During the same period patient was treated with ASPIRIN, SYNTHROID, PREDNISONE. Patient recovered.

Aspirin Side Effects Report #5486930-0
Pharmacist from UNITED STATES reported ASPIRIN problem on Oct 12, 2007. Male patient, 76 years of age, was diagnosed with coronary artery disease, prophylaxis, musculoskeletal pain and was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: gastric haemorrhage, gastrointestinal haemorrhage, gastrointestinal ulcer, helicobacter infection, . ASPIRIN dosage: 81MG EVERY DAY PO. During the same period patient was treated with SULINDAC. Patient was hospitalized. Patient recovered.

Thalomid Side Effects Report #5498416-8
THALOMID problem was reported by a Physician from UNITED STATES on Oct 19, 2007. Female patient, 76 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: fluid overload, gastrointestinal haemorrhage, gastrointestinal ulcer, pulmonary thrombosis, . THALOMID dosage: 200 MG, 4 IN 1 D, ORAL. During the same period patient was treated with ARIMIDEX, AREDIA, LOTREL, LASIX, SENOKOT, ASPIRIN, PROTONIX. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5451051-X
Consumer or non-health professional from UNITED KINGDOM reported REBIF problem on Aug 31, 2007. Female patient, 41 years of age, weighting 144.4 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: anaemia, gastrointestinal haemorrhage, gastrointestinal ulcer, injury, wound abscess, . REBIF dosage: unknown. During the same period patient was treated with AMITRIPTYLINE HYDROCHLORIDE, ACETAMINOPHEN W, ASCORBIC ACID. Patient was hospitalized. Patient recovered.

Naprosyn Side Effects Report #5326294-6
NAPROSYN problem was reported by a Pharmacist from UNITED STATES on May 14, 2007. Male patient, 63 years of age, weighting 186.0 lb, was diagnosed with sciatica and was treated with NAPROSYN. After drug was administered, patient experienced the following problems/side effects: diverticulum, gastrointestinal haemorrhage, gastrointestinal ulcer, . NAPROSYN dosage: 500MG BID PO (DURATION: SEVERAL MONTHS). Patient was hospitalized. Patient recovered.