Leuprolide and ascites Patient Reports February 12, 2012

Leuprolide Side Effects Report #5451803-6
Leuprolide side effect was reported by a Consumer or non-health professional from JAPAN on Sept 10, 2007. Female patient, 36 years of age, was diagnosed with uterine leiomyoma and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: abdominal adhesions, ascites, blood creatine phosphokinase increased. Leuprolide dosage: 3.75 MG (3.75 GM, 1 IN 28 D) SUBCUTANEOUS. Patient was hospitalized. Patient recovered.

Leuprolide Side Effects Report #4978986-6
Leuprolide side effect was reported by a Consumer or non-health professional from JAPAN on Mar 31, 2006. Male patient, 85 years of age, was diagnosed with prostate cancer  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, calcinosis, cholelithiasis, hepatic cyst, lymphadenopathy, pancreatitis, pleural effusion. Leuprolide dosage: 3.75 MG (3.75 MG, 1 IN 28 D) SUBCUTANEOUS. During the same period patient was treated with CASODEX, URSO, CHLORMADINONE ACETATE. Patient was hospitalized. Patient recovered.

Leuprolide Side Effects Report #5049220-6
Leuprolide side effect was reported by a Health Professional from AUSTRALIA on June 21, 2006. Male patient, 77 years of age, was diagnosed with prostate cancer  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: abdominal abscess, ascites, atelectasis, bacterial infection , bile duct cancer, bile duct stenosis, biliary sepsis, cholelithiasis, condition aggravated. Leuprolide dosage: 22.5 MG (22.5 MG,1 IN 3 M). During the same period patient was treated with ZOLEDRONIC ACID, NITRATE PATCH, ASPIRIN, CELECOXIB, SALBUTAMOL, NICORANDIL, VASOCARDOL CD. Patient was hospitalized. Patient died.

Leuprolide Side Effects Report #5081976-9
Leuprolide side effect was reported by a Consumer or non-health professional from AUSTRALIA on Aug 08, 2006. Male patient, 77 years of age, was diagnosed with prostate cancer  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, atelectasis, bacterial infection , bile duct cancer, bile duct stenosis, biliary sepsis, cellulitis , cholelithiasis, enterobacter infection. Leuprolide dosage: 22.5 MG (22.5 MG, 1 IN 3 M). During the same period patient was treated with ZOLEDRONIC ACID, NITRATE PATCH, ASPIRIN, CELECOXIB, ALBUTEROL SPIROS, NICORANDIL, VASOCARDOL CD. Patient was hospitalized. Patient died.


Leuprolide Side Effects Report #5422973-0
Leuprolide side effect was reported by a Consumer or non-health professional from GERMANY on Aug 15, 2007. Male patient, 69 years of age, was diagnosed with prostate cancer  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, blood bilirubin increased, fatigue, gamma-glutamyltransferase increased, hepatomegaly, liver function test abnormal, oedema, rash . Leuprolide dosage: 11.25 MG (11.25 MG, 1 IN 3 M); FOR YEARS. Patient was hospitalized. Patient recovered.

Leuprolide Side Effects Report #5177813-4
Leuprolide side effect was reported by a Consumer or non-health professional from HUNGARY on Dec 04, 2006. Male patient, 70 years of age, was diagnosed with neoplasm prostate and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, hepatic failure, oedema peripheral. Leuprolide dosage: 3.75 MG (3.75 MG,1 IN 1 M). During the same period patient was treated with FLUTAMIDE. Patient was hospitalized. Patient recovered.

Leuprolide Side Effects Report #5522468-X
Leuprolide side effect was reported by a Health Professional from ITALY on Nov 14, 2007. Female patient, 41 years of age, weighting 134.5 lb, was diagnosed with infertility  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, hydrothorax. Leuprolide dosage: unknown. Patient recovered.

Leuprolide Side Effects Report #5530865-1
Leuprolide side effect was reported by a Health Professional from ITALY on Nov 20, 2007. Female patient, 41 years of age, weighting 134.5 lb, was diagnosed with infertility  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, hydrothorax. Leuprolide dosage: unknown. Patient recovered.

Leuprolide Side Effects Report #5179016-6
Leuprolide side effect was reported by a Consumer or non-health professional from FRANCE on Dec 05, 2006. Female patient, 38 years of age, was diagnosed with in vitro fertilisation and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, dyspnoea, pleural effusion. Leuprolide dosage: 1.87 MG (1.87 MG, 1 IN 1 DOSE). During the same period patient was treated with GONAL, GONADOTROPHIN CHRORIONIC, UTROGESTAN. Patient was hospitalized. Patient recovered.


Leuprolide Side Effects Report #5197697-8
Leuprolide side effect was reported by a Consumer or non-health professional from FRANCE on Dec 22, 2006. Female patient, 38 years of age, was diagnosed with in vitro fertilisation and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, dyspnoea, ovarian hyperstimulation syndrome, pleural effusion. Leuprolide dosage: 1.87 MG (1.87 MG, 1 IN 1 ONCE), SUBCUTANEOUS/DAYS. During the same period patient was treated with GONAL, GONADOTROPHIN CHRORIONIC, UTROGESTAN. Patient recovered.

Leuprolide Side Effects Report #5362673-9
Leuprolide side effect was reported by a Consumer or non-health professional from JAPAN on June 12, 2007. Female patient, 45 years of age, was diagnosed with endometriosis  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: abdominal pain lower, acute abdomen, anorexia, ascites, genital haemorrhage, intestinal obstruction, intestinal perforation, intestinal stenosis, nausea . Leuprolide dosage: 1.88 MG (1.88 MG, 1 IN 28 D), SUBCUTANEOUS. During the same period patient was treated with LEUPROLIDE ACETATE. Patient was hospitalized. Patient recovered.

Leuprolide Side Effects Report #4914140-1
Leuprolide side effect was reported by a Physician from JAPAN on Feb 09, 2006. Female patient, 45 years of age, was diagnosed with endometriosis , gastrointestinal disorder and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: acute abdomen, anorexia, ascites, deep vein thrombosis , genital haemorrhage, ileal perforation, intestinal obstruction, intestinal stenosis, liver abscess. Leuprolide dosage: 1.88 MG (1.88 MG, 1 IN 28 D) SUBCUTANEOUS. During the same period patient was treated with LEUPROLIDE ACETATE, LEUPROLIDE ACETATE, LEUPROLIDE ACETATE. Patient was hospitalized. Patient recovered.

Leuprolide Side Effects Report #4939508-9
Leuprolide side effect was reported by a Consumer or non-health professional from JAPAN on Feb 24, 2006. Female patient, 45 years of age, was diagnosed with endometriosis  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, blood oestrogen increased, deep vein thrombosis , genital haemorrhage, intestinal obstruction, intestinal stenosis, liver abscess, peritonitis, post procedural complication. Leuprolide dosage: unknown. During the same period patient was treated with LEUPROLIDE ACETATE. Patient was hospitalized. Patient recovered.

Leuprolide Side Effects Report #5223683-5
Leuprolide side effect was reported by a Consumer or non-health professional from JAPAN on Jan 19, 2007. Female patient, 43 years of age, was diagnosed with endometriosis  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: abdominal distension, ascites, hypersensitivity. Leuprolide dosage: 3.75 MG (3.75 MG, 1 IN 28 D) SUBCUTANEOUS. Patient recovered.


Leuprolide Side Effects Report #5060305-0
Leuprolide side effect was reported by a Consumer or non-health professional from JAPAN on July 10, 2006. Female patient, 43 years of age, was diagnosed with endometriosis  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: abdominal distension, ascites. Leuprolide dosage: 3.75 MG (3.75 MG, 1 IN 28 D) SUBCUTANEOUS. Patient recovered.

Leuprolide Side Effects Report #5110042-9
Leuprolide side effect was reported by a Consumer or non-health professional from JAPAN on Sept 12, 2006. Female patient, 35 years of age, was diagnosed with endometriosis  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, blood pressure decreased, haemorrhagic ovarian cyst, ovarian cyst ruptured, proctalgia, vomiting. Leuprolide dosage: 1.88 MG (1.88 MG, 1 IN 28 D) SUBCUTANEOUS. Patient was hospitalized. Patient recovered.

Leuprolide Side Effects Report #5129262-2
Leuprolide side effect was reported by a Physician from JAPAN on Oct 06, 2006. Female patient, 35 years of age, was diagnosed with endometriosis  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, blood pressure decreased, ovarian cyst ruptured, vomiting. Leuprolide dosage: 1.88 MG (1.88MG, 1 IN 28 D) SUBCUTANEOUS. Patient recovered.

Leuprolide Side Effects Report #5080126-2
Leuprolide side effect was reported by a Health Professional from JAPAN on Aug 04, 2006. Female patient, 29 years of age, was diagnosed with endometriosis  and was treated with Leuprolide. After drug was administered, patient experienced the following side effects: abdominal distension, abdominal pain , ascites, c-reactive protein decreased, ovarian hyperstimulation syndrome. Leuprolide dosage: 1.88 MG (1.88 MG, 1 IN 28 D) SUBCUTANEOUS. Patient was hospitalized. Patient recovered.

Leuprolide Side Effects Report #4545344-8
Leuprolide side effect was reported by a Consumer or non-health professional from on Dec 29, 2004. Male patient was treated with Leuprolide. After drug was administered, patient experienced the following side effects: ascites, blood bilirubin increased, hepatic failure. Leuprolide dosage: 11.25 MG (11.25 MG, 1 IN 12 WK). During the same period patient was treated with LANSOPRAZOLE. Patient recovered.