Sandostatin and haemoglobin decreased Patient Reports February 11, 2012

Sandostatin Side Effects Report #4578425-3
Sandostatin side effect was reported by a Health Professional from on Feb 04, 2005. Female patient, 60 years of age, weighting 144.0 lb, was diagnosed with rectal cancer and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: anxiety , apnoea, blood sodium decreased, grand mal convulsion, haematocrit decreased, haemoglobin decreased, headache , injection site erythema, injection site swelling. Sandostatin dosage: 30MG. During the same period patient was treated with FLUOROURACIL, WELLBUTRIN, ALPRAZOLAM, QUININE, LISINOPRIL, PIROXICAM, HYDROCHLOROTHIAZIDE. Patient recovered.

Sandostatin Side Effects Report #4648637-9
Sandostatin side effect was reported by a Consumer or non-health professional from on Apr 22, 2005. Male patient, child 12 years of age, was diagnosed with pancreatitis, abdominal pain  and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: blood amylase increased, haemoglobin decreased, lipase increased, thrombocytopenia, thrombotic microangiopathy. Sandostatin dosage: unknown. During the same period patient was treated with PERFALGAN. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #6036263-9
Sandostatin side effect was reported by a Physician from CANADA on Jan 05, 2009. Male patient was diagnosed with metastatic neoplasm and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: gastrointestinal haemorrhage, haemoglobin decreased. Sandostatin dosage: 60 MG, QMO. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #5751608-2
Sandostatin side effect was reported by a Pharmacist from UNITED STATES on May 20, 2008. Female patient, 71 years of age, was diagnosed with meningioma and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: anaemia, cardiac failure, decubitus ulcer, haemoglobin decreased, infection , meningioma malignant, refusal of treatment by relative, wound secretion. Sandostatin dosage: 30 MG EVERY 28 DAYS. Patient was hospitalized. Patient died.


Sandostatin Side Effects Report #5721370-8
Sandostatin side effect was reported by a Health Professional from GERMANY on Apr 22, 2008. Female patient, 43 years of age, was diagnosed with medulloblastoma recurrent and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: blood bilirubin increased, blood lactate dehydrogenase increased, coombs negative haemolytic anaemia, fatigue, haemoglobin decreased, haptoglobin decreased, headache , platelet count decreased, red blood cell schistocytes present. Sandostatin dosage: 40 MG, QMO. During the same period patient was treated with SANDOSTATIN LAR, SANDOSTATIN LAR. Patient recovered.

Sandostatin Side Effects Report #5723162-2
Sandostatin side effect was reported by a Health Professional from GERMANY on Apr 22, 2008. Female patient, 43 years of age, was diagnosed with medulloblastoma recurrent and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: blood bilirubin increased, blood lactate dehydrogenase increased, coombs negative haemolytic anaemia, fatigue, haemoglobin decreased, haptoglobin decreased, headache , platelet count decreased, red blood cell schistocytes present. Sandostatin dosage: 40 MG, QMO. During the same period patient was treated with SANDOSTATIN LAR, SANDOSTATIN LAR. Patient recovered.

Sandostatin Side Effects Report #5836458-0
Sandostatin side effect was reported by a Consumer or non-health professional from CANADA on July 30, 2008. Female patient was diagnosed with hepatic neoplasm malignant and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: haemoglobin decreased, hepatic pain, transfusion. Sandostatin dosage: 20 MG ONCE A MONTH. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #5853692-4
Sandostatin side effect was reported by a Consumer or non-health professional from CANADA on Aug 14, 2008. Female patient was diagnosed with hepatic neoplasm malignant and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: haemoglobin decreased, hepatic neoplasm malignant, hepatic pain, transfusion. Sandostatin dosage: 20 MG ONCE A MONTH. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #5866312-X
Sandostatin side effect was reported by a Physician from JAPAN on Aug 26, 2008. Male patient was diagnosed with diarrhoea, graft versus host disease and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: blood potassium decreased, bradycardia, cardiac arrest , electrocardiogram st segment depression, haemoglobin decreased, hyperglycaemia, liver function test abnormal, loss of consciousness, scintigraphy. Sandostatin dosage: unknown. During the same period patient was treated with PROGRAF, NEUTROGIN, METHYLPREDNISOLONE SUCCINATE, METHYLPREDNISOLONE SUCCINATE, METHYLPREDNISOLONE SUCCINATE, HUMULIN R. Patient recovered.


Sandostatin Side Effects Report #5874487-1
Sandostatin side effect was reported by a Physician from JAPAN on Aug 26, 2008. Male patient was diagnosed with diarrhoea, graft versus host disease and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: blood lactate dehydrogenase increased, blood potassium decreased, bradycardia, cardiac arrest , electrocardiogram st segment depression, haemoglobin decreased, hyperglycaemia, liver function test abnormal, loss of consciousness. Sandostatin dosage: unknown. During the same period patient was treated with PROGRAF, NEUTROGIN, METHYLPREDNISOLONE SUCCINATE, METHYLPREDNISOLONE SUCCINATE, METHYLPREDNISOLONE SUCCINATE, HUMULIN R. Patient recovered.

Sandostatin Side Effects Report #5967689-7
Sandostatin side effect was reported by a Physician from JAPAN on Nov 20, 2008. Male patient was diagnosed with diarrhoea, graft versus host disease and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: blood lactate dehydrogenase increased, blood potassium decreased, bradycardia, cardiac arrest , electrocardiogram st segment depression, haemoglobin decreased, hyperglycaemia, liver function test abnormal, loss of consciousness. Sandostatin dosage: unknown. During the same period patient was treated with PROGRAF, NEUTROGIN, METHYLPREDNISOLONE SUCCINATE, METHYLPREDNISOLONE SUCCINATE, METHYLPREDNISOLONE SUCCINATE, HUMULIN R. Patient recovered.

Sandostatin Side Effects Report #4944976-2
Sandostatin side effect was reported by a Physician from UNITED STATES on Oct 18, 2005. Female patient, 65 years of age, weighting 140.0 lb, was diagnosed with carcinoid syndrome and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: application site pain, blood potassium decreased, diarrhoea, eating disorder , fatigue, flushing, haemoglobin decreased, occult blood positive, platelet count decreased. Sandostatin dosage: 20 MG; 30 MG; 40 MG, QMO, INJECTION NOS. During the same period patient was treated with SANDOSTATIN LAR, SANDOSTATIN LAR, INTRON, SYNTHROID, FOLIC ACID, LIPITOR, VITAPLEX. Patient recovered.

Sandostatin Side Effects Report #6124725-5
Sandostatin side effect was reported by a Consumer or non-health professional from CANADA on Mar 13, 2009. Female patient was diagnosed with carcinoid syndrome and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: blood pressure increased, body temperature decreased, dehydration, diarrhoea, fall , haemoglobin decreased. Sandostatin dosage: 30 MG, QMO. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #5931968-X
Sandostatin side effect was reported by a Consumer or non-health professional from ISRAEL on Oct 23, 2008. Female patient, 85 years of age, was diagnosed with acromegaly and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: anaphylactic reaction, ascites, haemoglobin decreased, ovarian cancer, paracentesis. Sandostatin dosage: 40 MG EVERY 28 DAYS. Patient was hospitalized. Patient recovered.


Sandostatin Side Effects Report #5938094-4
Sandostatin side effect was reported by a Physician from ISRAEL on Oct 30, 2008. Female patient, 85 years of age, was diagnosed with acromegaly and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: anaphylactic reaction, ascites, haemoglobin decreased, ovarian cancer, paracentesis. Sandostatin dosage: 40 MG EVERY 28 DAYS. During the same period patient was treated with ANTINEOPLASTIC AGENTS, TAXOL, CARBOPLATIN, GEMZAR. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #4913520-8
Sandostatin side effect was reported by a Physician from SWITZERLAND on Jan 27, 2006. Male patient, 21 years of age, was diagnosed with acromegaly and was treated with Sandostatin. After drug was administered, patient experienced the following side effects: haemoglobin decreased, pancytopenia, pericardial effusion, platelet count decreased, sinus bradycardia, ventricular hypertrophy, white blood cell count decreased. Sandostatin dosage: 50 MG, QMO. During the same period patient was treated with HYDROCORTISONE, ELTROXIN, TESTOVIRON. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #4750614-4
Sandostatin side effect was reported by a Consumer or non-health professional from FRANCE on Aug 11, 2005. Female patient, 54 years of age, was treated with Sandostatin. After drug was administered, patient experienced the following side effects: asthenia, dermatitis bullous, face oedema, haemoglobin decreased, inflammation, jaundice , malnutrition, nikolsky's sign, pruritus. Sandostatin dosage: unknown. During the same period patient was treated with RED BLOOD CELLS, BECILAN, BENERVA, MOPRAL, OSMOTAN, PLASMION, THIAMINE, VITAMIN B6. Patient was hospitalized. Patient recovered.

Sandostatin Side Effects Report #4764727-4
Sandostatin side effect was reported by a Consumer or non-health professional from FRANCE on Aug 11, 2005. Female patient, 54 years of age, was treated with Sandostatin. After drug was administered, patient experienced the following side effects: asthenia, dermatitis bullous, face oedema, haemoglobin decreased, inflammation, jaundice , malnutrition, nikolsky's sign, pruritus. Sandostatin dosage: unknown. During the same period patient was treated with RED BLOOD CELLS, BECILAN, BENERVA, OMEPRAZOLE, OSMOTAN, PLASMION, THIAMINE, VITAMIN B6. Patient was hospitalized. Patient recovered.