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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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Reported Creon Side Effects: hepatic enzyme increased, gastrooesophageal reflux disease, abdominal pain upper, steatorrhoea, malabsorption, amyotrophic lateral sclerosis, pancreatic insufficiency, proctitis ulcerative, henoch-schonlein purpura, lung neoplasm malignant, lethargy.
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Creon Side Effects Report #5197975-2
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 Side Effects Report #5234245-8
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.

Creon Side Effects Report #5253317-5
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 Side Effects Report #5257353-4
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.

Creon Side Effects Report #5281463-9
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 Side Effects Report #5284244-5
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.

Creon Side Effects Report #5095832-3
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 Side Effects Report #5408112-0
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.


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ALABAMA
ALASKA
AMERICAN SAMOA
ARIZONA
ARKANSAS
CALIFORNIA
COLORADO
CONNECTICUT
DELAWARE
DISTRICT OF COLUMBIA
FEDERATED STATES OF MICRONESIA
FLORIDA
GEORGIA
GUAM
HAWAII
IDAHO
ILLINOIS
INDIANA
IOWA
KANSAS
KENTUCKY
LOUISIANA
MAINE
MARSHALL ISLANDS
MARYLAND
MASSACHUSETTS
MICHIGAN
MINNESOTA
MISSISSIPPI
MISSOURI
MONTANA
NEBRASKA
NEVADA
NEW HAMPSHIRE
NEW JERSEY
NEW MEXICO
NEW YORK
NORTH CAROLINA
NORTH DAKOTA
NORTHERN MARIANA ISLANDS
OHIO
OKLAHOMA
OREGON
PALAU
PENNSYLVANIA
PUERTO RICO
RHODE ISLAND
SOUTH CAROLINA
SOUTH DAKOTA
TENNESSEE
TEXAS
UTAH
VERMONT
VIRGIN ISLANDS
VIRGINIA
WASHINGTON
WEST VIRGINIA
WISCONSIN
WYOMING
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