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BLOOD POTASSIUM ABNORMAL side effect

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Lisinopril Side Effects Report #5657808-4
Pharmacist from UNITED STATES reported LISINOPRIL problem on June 11, 2007. Female patient, 58 years of age, weighting 164.9 lb, was diagnosed with hypertension and was treated with LISINOPRIL. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, . LISINOPRIL dosage: unknown. During the same period patient was treated with TENORMIN. Patient recovered.

Symbicort Side Effects Report #5672887-6
SYMBICORT problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 07, 2007. Female patient, 25 years of age, weighting 158.1 lb, was diagnosed with asthma and was treated with SYMBICORT. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, depression, fatigue, headache, muscle spasms, paraesthesia, thirst, weight decreased, weight increased, . SYMBICORT dosage: unknown. During the same period patient was treated with TOPAMAX, SEROQUEL, ADDERALL, GUAIFENESIN, PROVENTIL, XOPENEX, ALLEGRA. Patient recovered.

Letairis Side Effects Report #5620642-5
Consumer or non-health professional from UNITED STATES reported LETAIRIS problem on Jan 31, 2008. Male patient, weighting 216.2 lb, was diagnosed with pulmonary hypertension and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, cardiac failure congestive, renal failure, . LETAIRIS dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, COUMADIN, ATENOLOL, OXYGEN, CIPROFLOXACIN, FISH OIL, DULCOLAX. Patient was hospitalized. Patient recovered.

Lenoxin Side Effects Report #5640906-9
LENOXIN problem was reported by a Pharmacist from GERMANY on Feb 18, 2008. Female patient, 17 years of age, weighting 108.0 lb, was diagnosed with oral contraception and was treated with LENOXIN. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, . LENOXIN dosage: .1875MG TWICE PER DAY. During the same period patient was treated with MIRANOVA, LOPIRIN. Patient recovered.


Letairis Side Effects Report #5601699-4
Consumer or non-health professional from UNITED STATES reported LETAIRIS problem on Jan 16, 2008. Male patient, weighting 216.2 lb, was diagnosed with pulmonary hypertension and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, cardiac failure congestive, dyspnoea, fluid overload, renal failure, . LETAIRIS dosage: unknown. During the same period patient was treated with LASIX, COUMADIN, ATENOLOL, OXYGEN, CIPROFLOXACIN, FISH OIL, DULCOLAX. Patient was hospitalized. Patient recovered.

Letairis Side Effects Report #5609502-3
LETAIRIS problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 22, 2008. Male patient, weighting 216.2 lb, was diagnosed with pulmonary hypertension and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, cardiac failure congestive, renal failure, . LETAIRIS dosage: unknown. During the same period patient was treated with SPIRONOLACTONE, COUMADIN, ATENOLOL, OXYGEN, CIPROFLOXACIN, FISH OIL, DULCOLAX. Patient was hospitalized. Patient recovered.

Coreg Side Effects Report #5554260-4
Consumer or non-health professional from UNITED STATES reported COREG CR problem on Dec 07, 2007. Female patient, 69 years of age, was treated with COREG CR. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, blood sodium abnormal, dizziness, vomiting, . COREG CR dosage: 20MG PER DAY. During the same period patient was treated with BENICAR, HYDROCHLOROTHIAZIDE, VITAMINS. Patient was hospitalized. Patient recovered.

Benicar Side Effects Report #5575630-4
BENICAR problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 17, 2007. Female patient, 69 years of age, was diagnosed with hypertension and was treated with BENICAR. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, blood sodium abnormal, dizziness, vomiting, . BENICAR dosage: (20 MG), PER ORAL. During the same period patient was treated with CARVEDILOL, HYDROCHLOROTHIAZIDE, VITAMIN. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5523004-4
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Nov 06, 2007. Female patient, 59 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, dizziness, excoriation, fall, foot fracture, hypotension, urinary tract infection, wrist fracture, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.


Byetta Side Effects Report #5575817-0
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on July 31, 2007. Female patient, 44 years of age, weighting 252.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, dyspnoea, food aversion, nausea, oedema peripheral, vomiting, . BYETTA dosage: unknown. During the same period patient was treated with EXENATIDE, CYMBALTA, METFORMIN, LASIX, LIPITOR, SINGULAIR. Patient recovered.

Coreg Side Effects Report #5486754-4
Consumer or non-health professional from UNITED STATES reported COREG problem on Oct 12, 2007. Male patient, 38 years of age, was treated with COREG. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, chest discomfort, chest pain, . COREG dosage: 6.25MG TWICE PER DAY. During the same period patient was treated with ARANESP, VENOFER, VITAMIN, LISINOPRIL, PROTINEX, NICODERM, REGLAN. Patient recovered.

Avonex Side Effects Report #5490171-0
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 04, 2007. Female patient, 59 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, fall, foot fracture, hypotension, thermal burn, urinary tract infection, wrist fracture, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Duragesic Side Effects Report #5444469-2
Consumer or non-health professional from UNITED STATES reported DURAGESIC problem on Aug 28, 2007. Female patient, weighting 110.0 lb, was diagnosed with pain and was treated with DURAGESIC. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, dehydration, detoxification, hyperhidrosis, muscle spasms, overdose, . DURAGESIC dosage: unknown. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5428512-2
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 13, 2007. Female patient, 59 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, excoriation, fall, foot fracture, hypotension, urinary tract infection, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.


Cisplatin Side Effects Report #5385264-2
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on July 09, 2007. Male patient, weighting 138.0 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, dehydration, fatigue, inadequate analgesia, malaise, pyrexia, . CISPLATIN dosage: 50 MG. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5385264-2
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on July 09, 2007. Male patient, weighting 138.0 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, dehydration, fatigue, inadequate analgesia, malaise, pyrexia, . CISPLATIN dosage: 50 MG. Patient was hospitalized. Patient recovered.

Metoprolol Side Effects Report #5710104-9
Consumer or non-health professional from UNITED STATES reported METOPROLOL SUCCINATE problem on Nov 26, 2007. Female patient, weighting 198.0 lb, was diagnosed with blood pressure and was treated with METOPROLOL SUCCINATE. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, dizziness, fall, nausea, vomiting, . METOPROLOL SUCCINATE dosage: unknown. During the same period patient was treated with LIPITOR, FEMARA, DILTIAZEM. Patient recovered.

Zinnat Side Effects Report #5712870-5
ZINNAT problem was reported by a Consumer or non-health professional from SPAIN on Apr 18, 2008. Male patient, child 6 years of age, was diagnosed with pharyngitis and was treated with ZINNAT. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, epstein-barr virus infection, hepatic failure, hepatomegaly, hepatotoxicity, lymphadenopathy, proteinuria, rash papular, rash pruritic, . ZINNAT dosage: 47MGK PER DAY. During the same period patient was treated with PARACETAMOL. Patient was hospitalized. Patient recovered.

Hydrodiuril Side Effects Report #5342815-1
Physician from SWITZERLAND reported HYDRODIURIL problem on May 24, 2007. Male patient, 78 years of age, was treated with HYDRODIURIL. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, ventricular tachycardia, . HYDRODIURIL dosage: unknown. During the same period patient was treated with ATENOLOL, PANTOPRAZOLE, ASPIRIN, ISOSORBIDE MONONITRATE, SPIRONOLACTONE, AMILORIDE, FUROSEMIDE. Patient recovered.


Zelnorm Side Effects Report #5333212-3
ZELNORM problem was reported by a Consumer or non-health professional from UNITED STATES on May 14, 2007. Female patient, 24 years of age, was diagnosed with impaired gastric emptying and was treated with ZELNORM. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, dehydration, nausea, urinary tract infection, vomiting, . ZELNORM dosage: 12 MG, TID. During the same period patient was treated with PRILOSEC, POTASSIUM CHLORIDE, PRENATAL VITAMINS, VERAPAMIL, PENICILLIN VK, MUCINEX, PROVIGIL, EFFEXOR. Patient was hospitalized. Patient recovered.

Seretide Side Effects Report #5269890-7
Consumer or non-health professional from RUSSIAN FEDERATION reported SERETIDE problem on Mar 09, 2007. Male patient, 71 years of age, was diagnosed with chronic obstructive pulmonary disease and was treated with SERETIDE. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, burning sensation mucosal, cardiac failure, cardiopulmonary failure, ill-defined disorder, oropharyngeal candidiasis, pneumonia, . SERETIDE dosage: unknown. During the same period patient was treated with BECLOMETHASONE DIPROPIONATE, BERODUAL, ATROVENT, PULMICORT. Patient died on 02/26/2007.

Seroquel Side Effects Report #5278102-X
SEROQUEL problem was reported by a Physician from UNITED STATES on Nov 03, 2005. Male patient, 25 years of age, weighting 177.0 lb, was diagnosed with bipolar disorder and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, dizziness, headache, overdose, sinus tachycardia, suicide attempt, . SEROQUEL dosage: 5600 MG [PO. During the same period patient was treated with LEXAPRO, WELLBUTRIN, TRILEPTAL. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5662856-4
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on Mar 11, 2008. Male patient, weighting 170.9 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, blood potassium abnormal, blood sodium abnormal, blood urea increased, dehydration, electrolyte imbalance, hypotension, oral intake reduced, . CISPLATIN dosage: 200 MG. During the same period patient was treated with ACETAMINOPHEN, ASPIRIN, CLARITIN, HYTRIN, LIPITOR. Patient was hospitalized. Patient recovered.

Elspar Side Effects Report #5608741-5
ELSPAR problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 29, 2008. Female patient, weighting 160.9 lb, was treated with ELSPAR. After drug was administered, patient experienced the following problems/side effects: blood culture positive, blood potassium abnormal, deep vein thrombosis, haemoglobin abnormal, hypocalcaemia, infection, jugular vein thrombosis, lymphopenia, mouth ulceration, . ELSPAR dosage: 36000 MILLION IU. During the same period patient was treated with METHOTREXATE. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5517523-4
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Nov 06, 2007. Male patient, 64 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, blood potassium abnormal, blood urine present, confusional state, depression, diarrhoea, feeling abnormal, heart rate increased, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Lotrel Side Effects Report #5483291-8
LOTREL problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 03, 2007. Female patient was diagnosed with hypertension and was treated with LOTREL. After drug was administered, patient experienced the following problems/side effects: asthenia, blood potassium abnormal, blood pressure fluctuation, . LOTREL dosage: unknown. Patient recovered.

Avonex Side Effects Report #5455930-9
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Sept 06, 2007. Female patient, 49 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: anaesthetic complication, blood potassium abnormal, nausea, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Seroquel Side Effects Report #5460394-5
SEROQUEL problem was reported by a Health Professional from UNITED STATES on July 13, 2007. Female patient, 30 years of age, was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: blood glucose abnormal, blood potassium abnormal, . SEROQUEL dosage: unknown. Patient recovered.

Imitrex Side Effects Report #5415520-0
Consumer or non-health professional from UNITED STATES reported IMITREX problem on Aug 09, 2007. Female patient, 40 years of age, weighting 425.5 lb, was treated with IMITREX. After drug was administered, patient experienced the following problems/side effects: aura, blood potassium abnormal, convulsion, disorientation, loss of consciousness, . IMITREX dosage: unknown. During the same period patient was treated with LOTREL, AZULFIDINE. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5430562-7
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 15, 2007. Female patient, 49 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: anaesthetic complication, blood potassium abnormal, glaucoma, nausea, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5394107-2
Consumer or non-health professional from UNITED STATES reported CISPLATIN problem on July 20, 2007. Male patient, weighting 138.0 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: asthenia, blood potassium abnormal, dehydration, fatigue, inadequate analgesia, malaise, pyrexia, weight decreased, . CISPLATIN dosage: 50 MG. Patient was hospitalized. Patient recovered.

Cisplatin Side Effects Report #5394107-2
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on July 20, 2007. Male patient, weighting 138.0 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: asthenia, blood potassium abnormal, dehydration, fatigue, inadequate analgesia, malaise, pyrexia, weight decreased, . CISPLATIN dosage: 50 MG. Patient was hospitalized. Patient recovered.

Digitek Side Effects Report #5726125-6
Consumer or non-health professional from UNITED STATES reported DIGITEK problem on May 01, 2008. Male patient, 32 years of age, weighting 90.00 lb, was diagnosed with cardiac disorder and was treated with DIGITEK. After drug was administered, patient experienced the following problems/side effects: anxiety, blood potassium abnormal, body temperature increased, fatigue, heart rate increased, renal impairment, . DIGITEK dosage: unknown. During the same period patient was treated with POLYSTYRENE SULFONATE, LANOXIN. Patient recovered.

Tysabri Side Effects Report #5735370-5
TYSABRI problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 30, 2008. Female patient, weighting 156.0 lb, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: anxiety, blood potassium abnormal, cardiac disorder, feeling abnormal, foot fracture, insomnia, memory impairment, mental disorder, mobility decreased, . TYSABRI dosage: unknown. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5373752-4
Consumer or non-health professional from UNITED STATES reported BETASERON problem on June 14, 2007. Male patient, 64 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, blood potassium abnormal, blood urine present, confusional state, depression, diarrhoea, feeling abnormal, heart rate increased, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Betaseron Side Effects Report #5333884-3
BETASERON problem was reported by a Consumer or non-health professional from UNITED STATES on May 14, 2007. Male patient, 64 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: atrial fibrillation, blood potassium abnormal, blood urine present, confusional state, depression, diarrhoea, feeling abnormal, heart rate increased, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.

Sulfamethoxalg Side Effects Report #5302057-2
Consumer or non-health professional from UNITED STATES reported SULFAMETHOXALG problem on Apr 16, 2007. Male patient, 91 years of age, weighting 151.0 lb, was diagnosed with nail infection and was treated with SULFAMETHOXALG. After drug was administered, patient experienced the following problems/side effects: blood potassium abnormal, cardiac disorder, cardiac fibrillation, dementia alzheimer's type, dysphagia, fall, hallucination, headache, . SULFAMETHOXALG dosage: unknown. During the same period patient was treated with LEVAQUIN. Patient died on 03/19/2007.

Forteo Side Effects Report #5630980-8
FORTEO problem was reported by a Physician from UNITED STATES on Feb 06, 2008. Female patient, weighting 159.5 lb, was diagnosed with osteoporosis, glaucoma, dyspnoea and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: anaemia, blood magnesium abnormal, blood potassium abnormal, glaucoma, haemorrhage, lupus pneumonitis, multiple fractures, multiple sclerosis, pericarditis, . FORTEO dosage: unknown. During the same period patient was treated with CELLCEPT, ACIPHEX, ALPHAGAN, BUSPAR, CARAFATE, DUONEB, FERROUS SULPHATE. Patient was hospitalized. Patient recovered.

Infergen Side Effects Report #5633635-9
Consumer or non-health professional from UNITED STATES reported INFERGEN problem on Jan 28, 2008. Female patient, weighting 339.5 lb, was diagnosed with hepatitis c and was treated with INFERGEN. After drug was administered, patient experienced the following problems/side effects: anaemia, blood chloride abnormal, blood potassium abnormal, blood sodium abnormal, electrolyte imbalance, . INFERGEN dosage: unknown. During the same period patient was treated with RIBAVIRIN, HUMALOG, LANTUS, ATENOLOL, LORAZEPAM. Patient was hospitalized. Patient recovered.

Infergen Side Effects Report #5640780-0
INFERGEN problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 28, 2008. Female patient, weighting 154.0 lb, was diagnosed with hepatitis c and was treated with INFERGEN. After drug was administered, patient experienced the following problems/side effects: anaemia, blood chloride abnormal, blood potassium abnormal, blood sodium abnormal, dyspnoea, electrolyte imbalance, . INFERGEN dosage: unknown. During the same period patient was treated with RIBAVIRIN, HUMALOG, LANTUS, ATENOLOL, LORAZEPAM. Patient was hospitalized. Patient recovered.

Chantix Side Effects Report #5594146-2
Consumer or non-health professional from UNITED STATES reported CHANTIX problem on Jan 04, 2008. Male patient, 59 years of age, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: blood chloride abnormal, blood glucose increased, blood potassium abnormal, blood pressure increased, vomiting, . CHANTIX dosage: unknown. Patient recovered.

Forteo Side Effects Report #5598823-9
FORTEO problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 14, 2008. Female patient was diagnosed with osteoporosis, glaucoma, dyspnoea and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: anaemia, blood magnesium abnormal, blood potassium abnormal, cardiac disorder, diabetes mellitus, dyspnoea, glaucoma, haemorrhage, lung disorder, . FORTEO dosage: unknown. During the same period patient was treated with CELLCEPT, ACIPHEX, ALPHAGAN, BUSPAR, CARAFATE, DUONEB, FERROUS SULPHATE. Patient was hospitalized. Patient recovered.

Sevoflurane Side Effects Report #5534181-3
Consumer or non-health professional from UNITED KINGDOM reported SEVOFLURANE problem on Nov 28, 2007. Male patient, 14 years of age, weighting 198.4 lb, was treated with SEVOFLURANE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus increased, blood potassium abnormal, cardiac arrest, creatinine renal clearance decreased, metabolic acidosis, rhabdomyolysis, . SEVOFLURANE dosage: unknown. During the same period patient was treated with SUPRANE, PROPOFOL, FENTANYL, DICLOFENAC, PARACETAMOL, MORPHINE, ONDANSETRON. Patient died on 09/08/2007.

Sevoflurane Side Effects Report #5571545-6
SEVOFLURANE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Dec 14, 2007. Male patient, 14 years of age, weighting 198.4 lb, was treated with SEVOFLURANE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus increased, blood potassium abnormal, cardiac arrest, creatinine renal clearance decreased, metabolic acidosis, rhabdomyolysis, . SEVOFLURANE dosage: unknown. During the same period patient was treated with SUPRANE, PROPOFOL, FENTANYL, DICLOFENAC, ACETAMINOPHEN, MORPHINE, ONDANSETRON. Patient died on 09/08/2007.

Sevoflurane Side Effects Report #5571549-3
Consumer or non-health professional from UNITED KINGDOM reported SEVOFLURANE problem on Dec 14, 2007. Male patient, 14 years of age, weighting 198.4 lb, was treated with SEVOFLURANE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus increased, blood potassium abnormal, cardiac arrest, creatinine renal clearance decreased, metabolic acidosis, rhabdomyolysis, . SEVOFLURANE dosage: unknown. During the same period patient was treated with SUPRANE, PROPOFOL, FENTANYL, DICLOFENAC, ACETAMINOPHEN, MORPHINE, ONDANSETRON. Patient died on 09/08/2007.

Sevoflurane Side Effects Report #5571584-5
SEVOFLURANE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Dec 14, 2007. Male patient, 14 years of age, weighting 198.4 lb, was treated with SEVOFLURANE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus increased, blood potassium abnormal, cardiac arrest, creatinine renal clearance decreased, metabolic acidosis, rhabdomyolysis, . SEVOFLURANE dosage: unknown. During the same period patient was treated with SUPRANE, PROPOFOL, FENTANYL, DICLOFENAC, ACETAMINOPHEN, MORPHINE, ONDANSETRON. Patient died on 09/08/2007.

Sevoflurane Side Effects Report #5512667-5
Consumer or non-health professional from UNITED KINGDOM reported SEVOFLURANE problem on Oct 31, 2007. Male patient, 14 years of age, weighting 198.4 lb, was treated with SEVOFLURANE. After drug was administered, patient experienced the following problems/side effects: blood calcium decreased, blood phosphorus increased, blood potassium abnormal, cardiac arrest, creatinine renal clearance decreased, metabolic acidosis, rhabdomyolysis, . SEVOFLURANE dosage: unknown. During the same period patient was treated with SUPRANE, PROPOFOL, FENTANYL, DICLOFENAC, PARACETAMOL, MORPHINE, ONDANSETRON. Patient died on 09/08/2007.

Zoledronic Side Effects Report #5519298-1
ZOLEDRONIC ACID problem was reported by a Physician from POLAND on Nov 14, 2007. Female patient, 80 years of age, weighting 160.7 lb, was diagnosed with osteoporosis postmenopausal and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: asthenia, blood creatinine abnormal, blood potassium abnormal, blood urea, c-reactive protein increased, cardiac failure chronic, cardiac failure congestive, concomitant disease progression, cough, . ZOLEDRONIC ACID dosage: unknown. During the same period patient was treated with CALCIUM, VITAMIN D, DICLOFENAC. Patient was hospitalized. Patient died on 10/08/2007.

Zoledronic Side Effects Report #5520244-5
Physician from POLAND reported ZOLEDRONIC ACID problem on Nov 14, 2007. Female patient, 80 years of age, weighting 160.7 lb, was diagnosed with osteoporosis postmenopausal and was treated with ZOLEDRONIC ACID. After drug was administered, patient experienced the following problems/side effects: asthenia, blood creatinine abnormal, blood potassium abnormal, blood urea, c-reactive protein increased, cardiac failure chronic, cardiac failure congestive, concomitant disease progression, cough, . ZOLEDRONIC ACID dosage: unknown. During the same period patient was treated with CALCIUM, VITAMIN D, DICLOFENAC. Patient was hospitalized. Patient died on 10/08/2007.

Cisplatin Side Effects Report #5489515-5
CISPLATIN problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 16, 2007. Female patient, weighting 127.4 lb, was treated with CISPLATIN. After drug was administered, patient experienced the following problems/side effects: asthenia, blood magnesium abnormal, blood potassium abnormal, culture urine positive, dizziness, dyspnoea, escherichia infection, hypovolaemia, mucosal dryness, . CISPLATIN dosage: 83 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, TAXOL. Patient was hospitalized. Patient recovered.

Ribavirin Side Effects Report #5451016-8
Consumer or non-health professional from UNITED STATES reported RIBAVIRIN problem on May 30, 2007. Female patient, 69 years of age, was diagnosed with hepatitis c and was treated with RIBAVIRIN. After drug was administered, patient experienced the following problems/side effects: anaemia, anorexia, blood potassium abnormal, cardiac disorder, dental caries, gingival bleeding, mouth haemorrhage, platelet count decreased, toothache, . RIBAVIRIN dosage: unknown. During the same period patient was treated with PEGINTERFERON ALFA, VALSARTAN, LEVOTHYROXINE, MILK THISTLE, ATENOLOL, DIURETIC. Patient was hospitalized. Patient recovered.