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CREON Safety Reports
Total CREON reports: 8.CREON FDA safety alerts: No.
Reported deaths: 1 Reported hospitalizations: 3.
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Consumer or non-health professional from ITALY reported CREON problem on Jan 02, 2007. Female patient was diagnosed with pancreatectomy, ill-defined disorder and was treated with CREON. After drug was administered, patient experienced the following problems/side effects: lethargy. CREON dosage: DAILY DOSE: 450 MILLIGRAM(S). During the same period patient was treated with TAVOR, SUPRADYN. Patient was hospitalized. Patient recovered.
CREON problem was reported by a Consumer or non-health professional from GERMANY on Feb 01, 2007. Female patient was diagnosed with pancreatic insufficiency, ill-defined disorder, leg amputation and was treated with CREON. After drug was administered, patient experienced the following problems/side effects: lung neoplasm malignant. CREON dosage: unknown. During the same period patient was treated with NOVAMIN, VALORON N DROPS, OPIPRAMOL NEURAX, ASS RATIO, DUSODRILTE. Patient died on 10/05/2006.
Physician from FRANCE reported CREON problem on Feb 16, 2007. Female patient, weighting 92.59 lb, was diagnosed with pseudomonas infection and was treated with CREON. After drug was administered, patient experienced the following problems/side effects: henoch-schonlein purpura. CREON dosage: unknown. During the same period patient was treated with EPHYNAL, PULMOZYME, URSOLVAN, ZITHROMAX, FORTUM, NEBCIN. Patient recovered.
CREON problem was reported by a Consumer or non-health professional from GERMANY on Feb 23, 2007. Male patient, weighting 163.1 lb, was diagnosed with pancreatic insufficiency and was treated with CREON. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, gastrooesophageal reflux disease, hepatic enzyme increased. CREON dosage: unknown. Patient recovered.
Consumer or non-health professional from GERMANY reported CREON problem on Mar 22, 2007. Female patient, weighting 121.3 lb, was diagnosed with irritable bowel syndrome and was treated with CREON. After drug was administered, patient experienced the following problems/side effects: proctitis ulcerative. CREON dosage: unknown. Patient recovered.
CREON problem was reported by a Physician from GERMANY on Mar 23, 2007. Male patient, weighting 163.1 lb, was diagnosed with pancreatic insufficiency and was treated with CREON. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, gastrooesophageal reflux disease, hepatic enzyme increased, pancreatic insufficiency. CREON dosage: unknown. Patient recovered.
Consumer or non-health professional from FRANCE reported CREON problem on Aug 22, 2006. Male patient, 67 years of age, was diagnosed with ill-defined disorder and was treated with CREON. After drug was administered, patient experienced the following problems/side effects: amyotrophic lateral sclerosis. CREON dosage: unknown. During the same period patient was treated with ASPIRIN, LODALES, PLAVIX. Patient was hospitalized. Patient recovered.
CREON problem was reported by a Pharmacist from UNITED KINGDOM on July 26, 2007. Male patient, weighting 9.79 lb, was diagnosed with cystic fibrosis, ill-defined disorder and was treated with CREON. After drug was administered, patient experienced the following problems/side effects: malabsorption, steatorrhoea. CREON dosage: unknown. During the same period patient was treated with DALIVIT, VITAMIN E, ACID BLOCKER. Patient was hospitalized. Patient recovered.