Menu

• Ask a Health Expert about BLOOD CREATINE INCREASED
• Post Your Side Effect related to BLOOD CREATINE INCREASED
• BLOOD CREATINE INCREASED and FDA Warnings
• BLOOD CREATINE INCREASED in Patients Wiki
• Report BLOOD CREATINE INCREASED in Drug Side Effect Survey

BLOOD CREATINE INCREASED side effect

What is BLOOD CREATINE INCREASED ?

A Health Expert wants to answer your question. Please provide details below.

Type your question here

 letters left

Novolog Side Effects Report #5646497-0
Health Professional from UNITED STATES reported NOVOLOG problem on Feb 19, 2008. Male patient, weighting 183.0 lb, was diagnosed with diabetes mellitus, renal cell carcinoma, nausea and was treated with NOVOLOG. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, hypoglycaemia, . NOVOLOG dosage: unknown. During the same period patient was treated with SUTENT, COMPAZINE, OXYCODONE, DILAUDID, ASPIRIN, DOXAZOSIN MESYLATE, ALBUTEROL, SPIRIVA. Patient was hospitalized. Patient recovered.

Xyrem Side Effects Report #5658075-8
XYREM problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 28, 2008. Female patient, 67 years of age, weighting 185.0 lb, was diagnosed with fatigue, fibromyalgia and was treated with XYREM. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood pressure increased, . XYREM dosage: 6 GM (3 MG, 2 IN 1 D), ORAL. Patient recovered.

Spironolactone Side Effects Report #5665005-1
Health Professional from UNITED KINGDOM reported SPIRONOLACTONE problem on Mar 03, 2008. Female patient, 72 years of age, was diagnosed with hypertension and was treated with SPIRONOLACTONE. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, bronchospasm, epistaxis, hyperkalaemia, nasal congestion, nausea, . SPIRONOLACTONE dosage: unknown. During the same period patient was treated with DOXAZOSIN MESYLATE, ATENOLOL, LISINOPRIL, ANTIHYPERTENSIVES, BENDROFLUMETHIAZIDE, FELODIPINE. Patient was hospitalized. Patient recovered.

Valaciclovir Side Effects Report #5678064-7
VALACICLOVIR HYDROCHLORIDELET problem was reported by a Physician from JAPAN on Mar 06, 2008. Female patient, 87 years of age, weighting 103.4 lb, was diagnosed with herpes zoster and was treated with VALACICLOVIR HYDROCHLORIDELET. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood urea increased, dyslalia, encephalopathy, muscular weakness, nausea, vomiting, . VALACICLOVIR HYDROCHLORIDELET dosage: 3000 MG/ PER DAY/ORAL. Patient was hospitalized. Patient recovered.


Thyrogen Side Effects Report #5622910-X
Physician from ARGENTINA reported THYROGEN problem on Jan 24, 2008. Female patient, 40 years of age, weighting 167.6 lb, was diagnosed with diagnostic procedure and was treated with THYROGEN. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood sodium decreased, blood thyroid stimulating hormone abnormal, blood urea abnormal, hyperkalaemia, nausea, vomiting, . THYROGEN dosage: unknown. During the same period patient was treated with CALCIUM CARBONATE. Patient was hospitalized. Patient recovered.

Clofarabine Side Effects Report #5629775-0
CLOFARABINE problem was reported by a Health Professional from FRANCE on Jan 31, 2008. Male patient, child 9 years of age, was diagnosed with acute lymphocytic leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood electrolytes abnormal, blood potassium decreased, blood sodium increased, blood urea increased, brain neoplasm malignant, computerised tomogram abnormal, convulsion, dyspnoea, . CLOFARABINE dosage: unknown. During the same period patient was treated with ETOPOSIDE, CYCLOPHOSPHAMIDE, TAZOCILLINE, AMIKIN, VANCOMYCIN. Patient died on 12/06/2007.

Acyclovir Side Effects Report #5630597-5
Consumer or non-health professional from NORWAY reported ACYCLOVIR problem on Feb 13, 2008. Male patient, 29 years of age, was treated with ACYCLOVIR. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, hallucination, visual, . ACYCLOVIR dosage: unknown. Patient recovered.

Lisinopril Side Effects Report #5643028-6
LISINOPRIL problem was reported by a Pharmacist from UNITED STATES on Feb 27, 2008. Male patient, 76 years of age, was diagnosed with hypertension and was treated with LISINOPRIL. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood urea increased, . LISINOPRIL dosage: 10MG EVERY DAY PO. Patient was hospitalized. Patient recovered.

Certican Side Effects Report #5643433-8
Physician from DENMARK reported CERTICAN problem on Jan 16, 2008. Male patient, 56 years of age, was diagnosed with lung transplant and was treated with CERTICAN. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood urea increased, dyspnoea, pulmonary embolism, pulmonary hypertension, . CERTICAN dosage: 0.5 MG, BID. During the same period patient was treated with SANDIMMUNE. Patient was hospitalized. Patient recovered.


Valtrex Side Effects Report #5644713-2
VALTREX problem was reported by a Consumer or non-health professional from UNITED STATES on June 26, 2007. Male patient was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, creatinine renal clearance decreased, . VALTREX dosage: unknown. During the same period patient was treated with CYTOVENE, EPZICOM, KALETRA, BACTRIM DS. Patient recovered.

Januvia Side Effects Report #5654658-X
Physician from UNITED STATES reported JANUVIA problem on Oct 24, 2007. Male patient was diagnosed with diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . JANUVIA dosage: unknown. During the same period patient was treated with ACTOS. Patient recovered.

Januvia Side Effects Report #5656626-0
JANUVIA problem was reported by a Physician from UNITED STATES on Dec 13, 2007. Female patient was diagnosed with diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . JANUVIA dosage: unknown. Patient recovered.

Revlimid Side Effects Report #5583865-X
Health Professional from UNITED STATES reported REVLIMID problem on Dec 21, 2007. Male patient, 79 years of age, weighting 166.9 lb, was diagnosed with chronic lymphocytic leukaemia and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, tumour lysis syndrome, . REVLIMID dosage: 2.5 MG, DAILY, ORAL. During the same period patient was treated with ALLOPURINOL, ANTIBIOTIC. Patient was hospitalized. Patient recovered.

Innohep Side Effects Report #5586166-9
INNOHEP problem was reported by a Physician from on Dec 20, 2007. Female patient, 69 years of age, weighting 147.7 lb, was diagnosed with atrial fibrillation and was treated with INNOHEP. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, malaise, nausea, syncope, . INNOHEP dosage: unknown. During the same period patient was treated with BISOPROLOL FUMARATE. Patient recovered.


Etoposide Side Effects Report #5597500-8
Health Professional from FRANCE reported ETOPOSIDE problem on Jan 11, 2008. Female patient, weighting 44.09 lb, was diagnosed with t-cell type acute leukaemia, analgesia, vomiting, prophylaxis, abdominal pain, oedema and was treated with ETOPOSIDE. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, hyponatraemia, renal failure acute, urinary retention, . ETOPOSIDE dosage: unknown. During the same period patient was treated with NALBUPHINE, METOPIMAZINE, CHLORPROMAZINE HYDROCHLORIDE, CEFTAZIDIME, PHLOROGLUCINOL, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Escitalopram Side Effects Report #5599630-3
ESCITALOPRAM problem was reported by a Health Professional from DENMARK on Jan 03, 2008. Female patient, 62 years of age, was diagnosed with musculoskeletal pain and was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, pancreatitis acute, pulmonary embolism, . ESCITALOPRAM dosage: unknown. During the same period patient was treated with BARACLUDE, RITUXAN, TERCIAN, NOCTRAN, DURAGESIC, DULCOLAX. Patient was hospitalized. Patient recovered.

Milk Side Effects Report #5601523-X
Consumer or non-health professional from UNITED STATES reported MILK OF MAGNESIA problem on Jan 09, 2008. Male patient, 78 years of age, weighting 194.0 lb, was diagnosed with constipation and was treated with MILK OF MAGNESIA. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . MILK OF MAGNESIA dosage: TOTAL DAILY DOSE: 22.5 ML UNIT DOSE: 15 ML. During the same period patient was treated with VITAMINS, PREDNISONE. Patient recovered.

Valtrex Side Effects Report #5604323-X
VALTREX problem was reported by a Physician from JAPAN on Jan 23, 2008. Female patient, 76 years of age, was diagnosed with herpes zoster and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood urea increased, dizziness, renal failure acute, . VALTREX dosage: 500MG THREE TIMES PER DAY. During the same period patient was treated with NORVASC. Patient was hospitalized. Patient recovered.

Verapamil Side Effects Report #5604457-X
Physician from UNITED STATES reported VERAPAMIL problem on Jan 07, 2008. Female patient, 89 years of age, was treated with VERAPAMIL. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood potassium increased, blood pressure decreased, blood urea increased, completed suicide, heart rate decreased, poisoning, . VERAPAMIL dosage: unknown. During the same period patient was treated with POTASSIUM CHLORIDE. Patient died.


Verapamil Side Effects Report #5605350-9
VERAPAMIL problem was reported by a Physician from UNITED STATES on Jan 07, 2008. Female patient, 51 years of age, was treated with VERAPAMIL. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood glucose increased, bradycardia, cardio-respiratory arrest, completed suicide, gastrointestinal sounds abnormal, nodal rhythm, poisoning, unresponsive to stimuli, . VERAPAMIL dosage: unknown. During the same period patient was treated with ALPRAZOLAM. Patient was hospitalized. Patient died.

Immune Side Effects Report #5609196-7
Health Professional from UNITED STATES reported IMMUNE CELLS problem on Jan 30, 2008. Male patient, 56 years of age, weighting 248.0 lb, was treated with IMMUNE CELLS. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood lactate dehydrogenase increased, blood urea increased, dehydration, electrolyte imbalance, fluid imbalance, haemoglobin decreased, haemolysis, hyponatraemia, . IMMUNE CELLS dosage: unknown. Patient was hospitalized. Patient recovered.

Propofol Side Effects Report #5627099-9
PROPOFOL problem was reported by a Pharmacist from UNITED STATES on Nov 13, 2007. Male patient, 18 years of age, weighting 275.6 lb, was diagnosed with acute respiratory distress syndrome and was treated with PROPOFOL. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . PROPOFOL dosage: 3-5MG/K/HR. During the same period patient was treated with MIDAZOLAM, FENTANY, REGLAN, NEXIUM. Patient was hospitalized. Patient recovered.

Tekturna Side Effects Report #5643989-5
Physician from UNITED STATES reported TEKTURNA problem on Oct 17, 2007. Male patient, 75 years of age, was treated with TEKTURNA. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . TEKTURNA dosage: 150 MG, QD, ORAL. Patient recovered.

Byetta Side Effects Report #5649762-6
BYETTA problem was reported by a Physician from UNITED STATES on Nov 13, 2007. Male patient, 87 years of age, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood urea increased, malaise, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, PRAVACHOL, UNVASC, ENALAPRIL MALEATE. Patient recovered.

Byetta Side Effects Report #5650750-4
Physician from UNITED STATES reported BYETTA problem on Dec 21, 2007. Male patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . BYETTA dosage: unknown. Patient recovered.

Byetta Side Effects Report #5650778-4
BYETTA problem was reported by a Physician from UNITED STATES on Dec 21, 2007. Female patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . BYETTA dosage: unknown. Patient recovered.

Ifosfamide Side Effects Report #5531402-8
Consumer or non-health professional from UNITED STATES reported IFOSFAMIDE problem on Nov 19, 2007. Female patient, 76 years of age, was diagnosed with sarcoma uterus, hypoalbuminaemia and was treated with IFOSFAMIDE. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, cerebrovascular disorder, encephalopathy, vaginal haemorrhage, . IFOSFAMIDE dosage: unknown. During the same period patient was treated with EPIRUBICIN. Patient recovered.

Milk Side Effects Report #5542455-5
MILK OF MAGNESIA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 27, 2007. Male patient, 78 years of age, weighting 194.0 lb, was diagnosed with constipation and was treated with MILK OF MAGNESIA. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . MILK OF MAGNESIA dosage: TOTAL DAILY DOSE: 22.5 ML UNIT DOSE: 15 ML. During the same period patient was treated with VITAMINS, PREDNISONE. Patient recovered.

Optiray Side Effects Report #5562835-1
Pharmacist from UNITED STATES reported OPTIRAY problem on Dec 03, 2007. Female patient was diagnosed with computerised tomogram and was treated with OPTIRAY. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood urea increased, . OPTIRAY dosage: 94 ML, SINGLE. Patient recovered.

Etoposide Side Effects Report #5574640-0
ETOPOSIDE problem was reported by a Health Professional from FRANCE on Dec 18, 2007. Female patient, weighting 44.09 lb, was diagnosed with t-cell type acute leukaemia, analgesia, vomiting, prophylaxis, abdominal pain, oedema and was treated with ETOPOSIDE. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, hyponatraemia, renal failure acute, urinary retention, . ETOPOSIDE dosage: unknown. During the same period patient was treated with NALBUPHINE, METOPIMAZINE, CHLORPROMAZINE HYDROCHLORIDE, CEFTAZIDIME, PHLOROGLUCINOL, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Velcade Side Effects Report #5580691-2
Physician from JAPAN reported VELCADE problem on Dec 20, 2007. Male patient, 77 years of age, weighting 143.3 lb, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood urea increased, disease progression, dyspnoea, metabolic acidosis, multiple myeloma, oedema, tumour lysis syndrome, weight increased, . VELCADE dosage: 1.60 MG, INTRAVENOUS. During the same period patient was treated with DEXAMETHASONE, FAMOTIDINE, SELBEX, BAKTAR, ALLOPURINOL, METHYCOBAL. Patient died on 08/03/2007.

Methotrexate Side Effects Report #5587697-8
METHOTREXATE problem was reported by a Pharmacist from UNITED STATES on Oct 30, 2007. Male patient, 18 years of age, weighting 207.2 lb, was diagnosed with bone sarcoma and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, mucosal inflammation, stomatitis, . METHOTREXATE dosage: unknown. During the same period patient was treated with BICARBONATE. Patient was hospitalized. Patient recovered.

Aprotinin Side Effects Report #5507452-4
Consumer or non-health professional from UNITED STATES reported APROTININ problem on Oct 31, 2007. Male patient, 72 years of age, was treated with APROTININ. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, renal impairment, renal tubular necrosis, thrombocytopenia, . APROTININ dosage: unknown. Patient was hospitalized. Patient recovered.

Aprotinin Side Effects Report #5507457-3
APROTININ problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 31, 2007. Male patient, 83 years of age, was treated with APROTININ. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood creatine phosphokinase increased, renal failure acute, renal tubular necrosis, . APROTININ dosage: unknown. Patient was hospitalized. Patient recovered.

Avandamet Side Effects Report #5512536-0
Consumer or non-health professional from UNITED STATES reported AVANDAMET problem on July 16, 2007. Male patient, 80 years of age, was treated with AVANDAMET. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood potassium increased, . AVANDAMET dosage: unknown. During the same period patient was treated with ALLEGRA, BECLOMETHASONE DIPROPIONATE, DIOVAN, ZOCOR, ZETIA, TOPROL, PROVENTIL GENTLEHALER, KAYEXALATE. Patient recovered.

Bisoprolol Side Effects Report #5512794-2
BISOPROLOL FUMARATE problem was reported by a Consumer or non-health professional from FRANCE on Nov 05, 2007. Female patient, 52 years of age, was diagnosed with cardiac failure, metastatic neoplasm and was treated with BISOPROLOL FUMARATE. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood pressure decreased, cardiac failure, condition aggravated, hypokinesia, mitral valve incompetence, . BISOPROLOL FUMARATE dosage: 1.25 MG (1.25 MG,1 IN 1 D) ORAL. During the same period patient was treated with CARVEDILOL. Patient was hospitalized. Patient recovered.

Ifosfamide Side Effects Report #5523496-0
Health Professional from ITALY reported IFOSFAMIDE problem on Nov 19, 2007. Female patient, 76 years of age, was diagnosed with sarcoma uterus, hypoalbuminaemia and was treated with IFOSFAMIDE. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, encephalopathy, vaginal haemorrhage, . IFOSFAMIDE dosage: unknown. During the same period patient was treated with EPIRUBICIN. Patient recovered.

Nevanac Side Effects Report #5525367-2
NEVANAC problem was reported by a Physician from UNITED STATES on Aug 15, 2007. Female patient, 56 years of age, weighting 138.0 lb, was diagnosed with chorioretinopathy, macular oedema and was treated with NEVANAC. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . NEVANAC dosage: unknown. During the same period patient was treated with PREDTE, WELLBUTRIN, DIAMOX, COSOPT, DACLIZUMAB, CYCLOSPORINE, PREDNISONE. Patient recovered.

Januvia Side Effects Report #5533576-1
Health Professional from UNITED STATES reported JANUVIA problem on Sept 06, 2007. Female patient was diagnosed with diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . JANUVIA dosage: 100 MG/DAILY/PO. Patient recovered.

Methotrexate Side Effects Report #5542520-2
METHOTREXATE problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 13, 2007. Male patient, 14 years of age, was diagnosed with juvenile arthritis and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, dehydration, vomiting, . METHOTREXATE dosage: 15MG/M2. During the same period patient was treated with DICLOFENAC, PREDNISOLONE. Patient recovered.

Byetta Side Effects Report #5558324-0
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Aug 30, 2007. Male patient was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE. Patient recovered.

Prinivil Side Effects Report #5478172-X
PRINIVIL problem was reported by a Pharmacist from UNITED STATES on Feb 13, 2007. Male patient, 62 years of age, was treated with PRINIVIL. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, . PRINIVIL dosage: unknown. During the same period patient was treated with IRBESARTAN, ASPIRIN, CILOSTAZOL, DARBEPOETIN ALFA, FOLIC ACID, FUROSEMIDE, GABAPENTIN, GLYBURIDE. Patient was hospitalized. Patient recovered.

Benicar Side Effects Report #5481772-4
Physician from UNITED STATES reported BENICAR problem on Sept 24, 2007. Male patient, 72 years of age, weighting 276.0 lb, was diagnosed with hypertension and was treated with BENICAR. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood potassium increased, blood urea increased, hypotension, laboratory test abnormal, . BENICAR dosage: 20 MG (20 MG, 1 IN 1 D), PER ORAL. During the same period patient was treated with LISINOPRIL, FUROSEMIDE, COUMADIN, GEMFIBROZIL, NIFEDIPINE ER, SIMVASTATIN, GLIPIZIDE. Patient was hospitalized. Patient recovered.

Actonel Side Effects Report #5483172-X
ACTONEL problem was reported by a Health Professional from FRANCE on Sept 27, 2007. Female patient, 93 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood urea increased, dehydration, eating disorder, hypernatraemia, somnolence, . ACTONEL dosage: unknown. During the same period patient was treated with OLMESARTAN MEDOXOMIL, RISPERDAL, KARDEGIC. Patient was hospitalized. Patient died on 08/02/2007.

Nadolol Side Effects Report #5491849-5
Physician from UNITED STATES reported NADOLOL problem on Oct 05, 2007. Male patient, 61 years of age, was treated with NADOLOL. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood pressure decreased, blood urea increased, disorientation, haematocrit decreased, haemoglobin decreased, lethargy, nodal rhythm, sinus arrest, . NADOLOL dosage: 40 MG; DAILY. During the same period patient was treated with DILTIAZEM HYDROCHLORIDE, HYDROCHLOROTHIAZIDE, IRBESARTAN. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5495270-5
PROGRAF problem was reported by a Health Professional from UNITED STATES on Oct 08, 2007. Male patient, 36 years of age, was diagnosed with prophylaxis against transplant rejection and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, clostridium difficile colitis, cytomegalovirus enterocolitis, dyspepsia, . PROGRAF dosage: ORAL; 2 MG, BID, ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, PREDNISONE, ALLOPURINOL, PROCARDIA, COREG, COLCHICUM JTL LIQ, LIPITOR. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5504859-6
Consumer or non-health professional from UNITED STATES reported PROGRAF problem on Oct 19, 2007. Female patient, 70 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, hypovolaemia, . PROGRAF dosage: 5.5 MG, BID; ORAL. During the same period patient was treated with MYCOPHENOLATE MOFETIL, BACTRIM, IRON, LOPRESSOR, PROTONIX, LASIX, COLACE, IPRATROPIUM BROMIDE. Patient was hospitalized. Patient recovered.

Aprotinin Side Effects Report #5441675-8
APROTININ problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 22, 2007. Male patient, 72 years of age, was treated with APROTININ. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, renal impairment, renal tubular necrosis, thrombocytopenia, . APROTININ dosage: unknown. Patient was hospitalized. Patient recovered.

Aprotinin Side Effects Report #5441678-3
Consumer or non-health professional from UNITED STATES reported APROTININ problem on Aug 22, 2007. Male patient, 83 years of age, was treated with APROTININ. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood creatine phosphokinase increased, renal failure acute, renal tubular necrosis, . APROTININ dosage: unknown. Patient was hospitalized. Patient recovered.

Prezista Side Effects Report #5444581-8
PREZISTA problem was reported by a Physician from UNITED KINGDOM on Aug 28, 2007. Male patient, weighting 143.3 lb, was diagnosed with hiv infection, lipids increased and was treated with PREZISTA. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, haematuria, myalgia, . PREZISTA dosage: unknown. During the same period patient was treated with ETRAVIRINE, TRUVADA, FENOFIBRATE. Patient recovered.

Fabrazyme Side Effects Report #5463817-0
Physician from UNITED STATES reported FABRAZYME problem on Sept 07, 2007. Male patient, 62 years of age, was diagnosed with fabry's disease, polyuria and was treated with FABRAZYME. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood potassium decreased, blood urea increased, cardiac failure congestive, . FABRAZYME dosage: 70 MG Q2WKS IV. During the same period patient was treated with LASIX, COUMADIN, COREG, ZANTAC, LORTAB, KLONOPIN. Patient was hospitalized. Patient recovered.