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BLOOD UREA NITROGEN/CREATININE RATIO INCREASED side effect

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Lipitor Side Effects Report #5513430-1
Physician from UNITED STATES reported LIPITOR problem on Nov 06, 2007. Female patient, weighting 155.0 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: blood urea nitrogen/creatinine ratio increased, electrolyte imbalance, hallucination, hip fracture, hypoaesthesia, hyponatraemia, muscle spasms, myalgia, oedema peripheral, . LIPITOR dosage: unknown. During the same period patient was treated with CRESTOR, LANTUS, HUMALOG, CYMBALTA, SYNTHROID, TOPROL, LASIX, ACETYLSALICYLIC ACID SRT. Patient was hospitalized. Patient recovered.

Chantix Side Effects Report #5732401-3
CHANTIX problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 26, 2008. Female patient, weighting 168.0 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: blood urea nitrogen/creatinine ratio increased, weight increased, . CHANTIX dosage: unknown. Patient recovered.

Chantix Side Effects Report #5740931-3
Physician from UNITED STATES reported CHANTIX problem on May 08, 2008. Female patient, weighting 180.8 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: back pain, blood urea nitrogen/creatinine ratio increased, body temperature increased, chills, depression, ear pain, eye pain, mood altered, . CHANTIX dosage: unknown. Patient recovered.

Furosemide Side Effects Report #5377029-2
FUROSEMIDE problem was reported by a Pharmacist from UNITED STATES on June 28, 2007. Male patient, 85 years of age, was diagnosed with cardiac failure congestive and was treated with FUROSEMIDE. After drug was administered, patient experienced the following problems/side effects: asthenia, blood urea nitrogen/creatinine ratio increased, hypokalaemia, hypotension, . FUROSEMIDE dosage: 80MG BID PO. During the same period patient was treated with METOLAZONE. Patient was hospitalized. Patient recovered.


Januvia Side Effects Report #5293350-0
Health Professional from UNITED STATES reported JANUVIA problem on Apr 05, 2007. Female patient, 84 years of age, weighting 185.2 lb, was diagnosed with diabetes mellitus, lipids, hypertension and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: blood triglycerides increased, blood urea nitrogen/creatinine ratio increased, carbon dioxide decreased, chills, dyspnoea, oedema peripheral, . JANUVIA dosage: unknown. During the same period patient was treated with ACTOS, GLIMEPIRIDE, ZETIA, HYZAAR, ATENOLOL. Patient recovered.

Byetta Side Effects Report #5649197-6
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 10, 2007. Male patient, 67 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: albumin urine present, blood glucose increased, blood urea nitrogen/creatinine ratio increased, feeling abnormal, nausea, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, GLUCOPHAGE, AVANDIA. Patient recovered.

Byetta Side Effects Report #5576904-3
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Sept 26, 2007. Male patient, 67 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: albumin urine present, blood glucose increased, blood urea nitrogen/creatinine ratio increased, . BYETTA dosage: unknown. During the same period patient was treated with GLUCOPHAGE, AVANDIA. Patient recovered.

Humira Side Effects Report #5760265-0
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on May 29, 2008. Female patient, weighting 210.2 lb, was diagnosed with rheumatoid arthritis, blood pressure, diabetes mellitus, gastrooesophageal reflux disease, fibromyalgia, hypersensitivity, vitamin supplementation, anxiety and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: albumin globulin ratio decreased, blood chloride decreased, blood urea nitrogen/creatinine ratio increased, injection site irritation, injection site pain, intervertebral disc protrusion, mean platelet volume decreased, white blood cell count increased, . HUMIRA dosage: unknown. During the same period patient was treated with ATENOLOL, INSULIN GLARGINE, ESOMEPRAZOLE MAGNESIUM, PREGABALIN, MONTELUKAST, FOLIC ACID, LORAZEPAM. Patient was hospitalized. Patient recovered.