BLOOD POTASSIUM INCREASED side effect
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Drugs associated with BLOOD POTASSIUM INCREASED
ACYCLOVIR ADIRO ADVIL ALDACTONE ALEVE ALTACE AMARYL AMBISOME AMEVIVE AMILORIDE AMINO AMIODARONE AMISULPRIDE AMITRIPTYLINE AMLODIPINE ANAGRELIDE ARICEPT ASPIRIN ATENOLOL AUGMENTIN AVANDAMET AVANDIA AVAPRO AVASTIN AVONEX BACTRIM BACTROBAN BENICAR BETASERON BEVACIZUMAB BICITRA BISOPROLOL BLOPRESS BUFFERIN BUMETANIDE BUMEX BYETTA CAMPATH CAMPTO CARBOPLATIN CARIMUNE CERTICAN CHAMPIX CHANTIX CILOSTAZOL CIPRALEX CIPROFLOXACIN CISAPRIDE CISPLATIN CITALOPRAM CITRUCEL CLINDAMYCIN CLOFARABINE CLOZARIL COAPROVEL COMMIT COREG CORGARD COUMADIN COZAAR CRESTOR CYCLOSPORINE CYSTAGON CYTARABINE DAONIL DIAZEPAM DICLOFENAC DIFLUCAN DIGOXIN DILANTIN DIOVAN DOCETAXEL DOXORUBICIN DUROTEP ELITEK ENABLEX ENALAPRIL ENDOXAN ENTOCORT EPLERENONE ERAXIS ERYTHROMYCIN ESCITALOPRAM EXJADE FEMARA FENTANYL FLUDARABINE FORTEO FOSAMAX FOSINOPRIL FUROSEMIDE GABAPEN GEMCITABINE GEODON GLEEVEC HEPARIN HESPAN HUMALOG HUMULIN HYDROCHLOROTHIAZ HYDRODIURIL HYZAAR IBUPROFEN INDOCIN INNOHEP INSULIN ISOFLURANE ISOPTIN ISOSORBIDE JANUMET JANUVIA KADIAN KALETRA KETEK LAMISIL LANTUS LASIX LETAIRIS LEUCOVORIN LEVAQUIN LEVEMIR LEVOTHYROXINE LIPITOR LISINOPRIL LITHIUM LITHOBID LOCHOL LODOZ LOSARTAN LOTREL LYRICA MERCAPTAMINE METFORMIN METHOTREXATE METHYLENE MICARDIS MIDAMOR MIMPARA MIRALAX MIRENA MIRTAZAPINE MOBIC MODURETIC MONOPRIL MONURIL MONUROL MORPHINE MYCOPHENOLATE MYCOPHENOLIC NAPROXEN NARCAN NATEGLINIDE NEORAL NEXAVAR NIFEDIPINE NORVASC NOVOSEVEN OLMESARTAN OMEPRAZOLE OMNIPAQUE OPANA ORENCIA ORIGINAL ORLISTAT ORTHO OVIDREL OXYCODONE PAROXETINE PEGASYS PEPCID PHILLIPS PHOSPHOSODA PLAVIX POLYETHYLENE POTASSIUM PRAVASTATIN PREDNISONE PRINIVIL PROCRIT PROGRAF PROPAFENONE QUESTRAN QUILONUM RAPAMUNE RASILEZ REBIF REMICADE RENAGEL RENITEC REVLIMID RITALIN RITUXAN RITUXIMAB SANDOSTATIN SEROQUEL SOTAHEXAL SPIRIVA SPIRONOLACTONE STARSIS SUCCINYLCHOLINE SULFAMETHOXAZOLE SUNITINIB SYMLIN SYNAGIS TAGAMET TAMOXIFEN TARCEVA TEGRETOL TEKTURNA TEMODAL TEMODAR TEMOZOLOMIDE TENORMIN TERNELIN THALIDOMIDE THALOMID THYMOGLOBULIN TOPROL TORADOL TORSEMIDE TRASYLOL TRILEPTAL TRIMETHOPRIM TRISENOX TRUVADA ULTRAM VALSARTAN VALTREX VASOTEC VELCADE VERAPAMIL VESICARE VIAGRA VIRAMUNE XANAX XOLAIR YASMIN ZESTRIL ZOCOR ZOMETA ZONISAMIDE ZYPREXA ZYVOXForteo Side Effects Report #5648860-0
Physician from SPAIN reported FORTEO problem on Feb 27, 2008. Female patient, 60 years of age, was diagnosed with osteoporotic fracture and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, carbohydrate antigen 19-9 increased, echinococciasis, weight decreased, . FORTEO dosage: unknown. Patient recovered.
Symlin Side Effects Report #5649831-0
SYMLIN problem was reported by a Physician from UNITED STATES on Feb 21, 2008. Female patient, 63 years of age, weighting 348.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with SYMLIN. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, dyspnoea, lethargy, nausea, renal failure acute, weight decreased, . SYMLIN dosage: unknown. During the same period patient was treated with LANTUS, HUMALOG, SEPTRA, LEXAPRO, SYNTHROID, PRINIVIL, METOPROLOL TARTRATE, ZOCOR. Patient was hospitalized. Patient recovered.
Gabapen Side Effects Report #5661414-5
Physician from JAPAN reported GABAPEN problem on Feb 28, 2008. Female patient, 63 years of age, was diagnosed with pain management and was treated with GABAPEN. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . GABAPEN dosage: DAILY DOSE:600MG. Patient recovered.
Novoseven Side Effects Report #5671043-5
NOVOSEVEN problem was reported by a Health Professional from UNITED STATES on Mar 17, 2008. Male patient was treated with NOVOSEVEN. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, cyanosis, hypertension, hypotension, ventricular tachycardia, . NOVOSEVEN dosage: 0.12MG X1 IV. During the same period patient was treated with VASOPRESSIN, DOPAMINE, DOBUTAMINE, VECURONIUM BROMIDE, VANCOMYCIN, CEFTAZIDIME, CLINDAMYCIN, CALCIUM CHLORIDE. Patient recovered.
Zyprexa Side Effects Report #5672140-0
Physician from UNITED STATES reported ZYPREXA problem on Mar 06, 2008. Female patient, weighting 112.0 lb, was diagnosed with schizophrenia, paranoid type, agitation and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, coronary artery disease, electrocardiogram qt prolonged, left ventricular hypertrophy, mental disorder, . ZYPREXA dosage: 5 MG, EACH MORNING. During the same period patient was treated with ZYPREXA ZYDIS, HALOPERIDOL DECANOATE. Patient was hospitalized. Patient recovered.
Altace Side Effects Report #5672792-5
ALTACE problem was reported by a Physician from UNITED STATES on Sept 14, 2007. Female patient was treated with ALTACE. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . ALTACE dosage: 2.5 MG. Patient recovered.
Daonil Side Effects Report #5676845-7
Consumer or non-health professional from reported DAONIL problem on Mar 17, 2008. Female patient, 85 years of age, was diagnosed with diabetes mellitus, essential hypertension and was treated with DAONIL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, renal failure, . DAONIL dosage: unknown. During the same period patient was treated with GLUCOPHAGE, ENALAPRIL MALEATE. Patient was hospitalized. Patient recovered.
Spiriva Side Effects Report #5677716-2
SPIRIVA problem was reported by a Physician from UNITED STATES on Mar 20, 2008. Male patient, 60 years of age, weighting 302.0 lb, was diagnosed with chronic obstructive pulmonary disease, post-traumatic stress disorder and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, inflammation, prostatic disorder, prostatomegaly, protein total increased, . SPIRIVA dosage: unknown. Patient was hospitalized. Patient recovered.
Campto Side Effects Report #5679358-1
Consumer or non-health professional from JAPAN reported CAMPTO problem on Mar 13, 2008. Male patient was diagnosed with non-small cell lung cancer, hypertension, diarrhoea and was treated with CAMPTO. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, haemoglobin decreased, neutrophil count decreased, white blood cell count decreased, . CAMPTO dosage: DAILY DOSE:145MG. During the same period patient was treated with ENALAPRIL MALEATE, LOPERAMIDE HYDROCHLORIDE, URSO, BICARBONATE, HANGE. Patient recovered.
Spironolactone Side Effects Report #5682475-3
SPIRONOLACTONE problem was reported by a Pharmacist from UNITED STATES on Mar 26, 2008. Male patient, weighting 192.0 lb, was diagnosed with hypertension, oedema and was treated with SPIRONOLACTONE. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . SPIRONOLACTONE dosage: 50MG PO DAILY. During the same period patient was treated with BACTRIM, SIROLIMUS, MYCOPHENOLATE MOFETIL, FUROSEMIDE, ESCITALOPRAM OXALATE, OXYCODONE AND ACETAMINOPHEN. Patient was hospitalized. Patient recovered.
Trimethoprim Side Effects Report #5682700-9
Consumer or non-health professional from UNITED STATES reported TRIMETHOPRIM problem on Mar 26, 2008. Male patient, 41 years of age, weighting 330.7 lb, was diagnosed with infection, ulcer, wound and was treated with TRIMETHOPRIM. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . TRIMETHOPRIM dosage: unknown. During the same period patient was treated with HYDROMORPHONE, CEFEPIME, LASIX, KETOROLAC, IBUPROFEN, WARFARIN. Patient recovered.
Kadian Side Effects Report #5688161-8
KADIAN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 13, 2008. Male patient, 66 years of age, was diagnosed with cancer pain and was treated with KADIAN. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, renal impairment, . KADIAN dosage: 20 MG, 1 CAP DAILY, PER ORAL. During the same period patient was treated with LOXOPROFEN, DICLOFENAC. Patient recovered.
Avonex Side Effects Report #5615238-5
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Jan 22, 2008. Female patient, 50 years of age, weighting 155.0 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, diabetes mellitus, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Letairis Side Effects Report #5623852-6
LETAIRIS problem was reported by a Health Professional from UNITED STATES on Feb 07, 2008. Female patient, weighting 148.1 lb, was diagnosed with pulmonary hypertension, essential hypertension, hypercholesterolaemia and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . LETAIRIS dosage: unknown. During the same period patient was treated with REVATIO, SPIRONOLACTONE, COUMADIN, TOPROL, CARTIA XT, GEMFIBROZIL, ZOCOR, PREMARIN. Patient died.
Methotrexate Side Effects Report #5625523-9
Health Professional from UNITED STATES reported METHOTREXATE problem on Feb 11, 2008. Female patient, 49 years of age, weighting 515.9 lb, was diagnosed with psoriasis and was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, dialysis, pancytopenia, renal failure acute, therapeutic agent toxicity, . METHOTREXATE dosage: 2.5MG SIX TIMES A DAY PO. During the same period patient was treated with CYCLOSPORINE, CEFEPIME, METHADONE, INSULIN, PRILOSEC, EFFEXOR, WELLBUTRIN, FERROUS SULPHATE. Patient died on 11/27/2007.
Letairis Side Effects Report #5627831-4
LETAIRIS problem was reported by a Health Professional from UNITED STATES on Feb 11, 2008. Female patient, weighting 148.1 lb, was diagnosed with pulmonary hypertension, essential hypertension, hypercholesterolaemia and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . LETAIRIS dosage: unknown. During the same period patient was treated with REVATIO, COUMADIN, ALDACTONE, LASIX, TOPROL, CARTIA XT, GEMFIBROZIL, ZOCOR. Patient was hospitalized. Patient died.
Lisinopril Side Effects Report #5628634-7
Pharmacist from UNITED STATES reported LISINOPRIL problem on Feb 14, 2008. Male patient, 59 years of age, was diagnosed with hypertension and was treated with LISINOPRIL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . LISINOPRIL dosage: 20MG EVERY DAY PO. Patient recovered.
Ortho Side Effects Report #5630196-5
ORTHO EVRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 06, 2008. Female patient, weighting 97.00 lb, was diagnosed with menstruation irregular and was treated with ORTHO EVRA. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, metrorrhagia, mitral valve incompetence, mitral valve prolapse, myocardial infarction, off label use, stress cardiomyopathy, thyroid neoplasm, . ORTHO EVRA dosage: unknown. Patient was hospitalized. Patient recovered.
Acyclovir Side Effects Report #5630594-X
Consumer or non-health professional from UNITED KINGDOM reported ACYCLOVIR problem on Feb 18, 2008. Female patient, 79 years of age, weighting 220.5 lb, was treated with ACYCLOVIR. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, renal failure acute, . ACYCLOVIR dosage: 2850MG PER DAY. During the same period patient was treated with ASPIRIN, LANSOPRAZOLE, PHENYTOIN. Patient recovered.
Neoral Side Effects Report #5632963-0
NEORAL problem was reported by a Physician from JAPAN on Feb 18, 2008. Male patient, 80 years of age, was diagnosed with interstitial lung disease and was treated with NEORAL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, hepatic function abnormal, interstitial lung disease, . NEORAL dosage: 150 MG/D. During the same period patient was treated with PREDONINE, FAMOTIDINE, LASIX, WARFARIN. Patient died on 01/21/2007.
Lipitor Side Effects Report #5635546-1
Pharmacist from JAPAN reported LIPITOR problem on Feb 13, 2008. Male patient, 72 years of age, was diagnosed with hypercholesterolaemia and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . LIPITOR dosage: unknown. During the same period patient was treated with LASIX. Patient recovered.
Forteo Side Effects Report #5636455-4
FORTEO problem was reported by a Physician from SPAIN on Feb 11, 2008. Female patient, 60 years of age, was diagnosed with osteoporotic fracture and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, carcinoembryonic antigen increased, echinococciasis, weight decreased, . FORTEO dosage: unknown. Patient recovered.
Byetta Side Effects Report #5639236-0
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Feb 15, 2008. Female patient was diagnosed with diabetes mellitus, cardiac disorder and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, myocardial infarction, renal disorder, . BYETTA dosage: unknown. During the same period patient was treated with GLIPIZIDE. Patient was hospitalized. Patient recovered.
Symlin Side Effects Report #5639522-4
SYMLIN problem was reported by a Physician from UNITED STATES on Feb 08, 2008. Female patient, 63 years of age, weighting 348.0 lb, was diagnosed with type 2 diabetes mellitus and was treated with SYMLIN. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, dyspnoea, lethargy, nausea, renal failure acute, weight decreased, . SYMLIN dosage: unknown. During the same period patient was treated with LANTUS, HUMALOG, BACTRIM, LEXAPRO, SYNTHROID, PRINIVIL, METOPROLOL TARTRATE, ZOCOR. Patient was hospitalized. Patient recovered.
Valtrex Side Effects Report #5644886-1
Consumer or non-health professional from UNITED STATES reported VALTREX problem on Oct 01, 2007. Female patient, 61 years of age, was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, dizziness, palpitations, . VALTREX dosage: 250MG PER DAY. Patient recovered.
Diovan Side Effects Report #5662197-5
DIOVAN problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 28, 2007. Female patient was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . DIOVAN dosage: 80 MG. Patient recovered.
Toradol Side Effects Report #5662556-0
Consumer or non-health professional from UNITED STATES reported TORADOL problem on Feb 22, 2007. Female patient, 83 years of age, was treated with TORADOL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, renal failure acute, . TORADOL dosage: unknown. Patient recovered.
Diovan Side Effects Report #5662773-X
DIOVAN problem was reported by a Physician from UNITED STATES on Apr 03, 2007. Female patient was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . DIOVAN dosage: 80MG. Patient recovered.
Lamisil Side Effects Report #5579132-0
Physician from JAPAN reported LAMISIL problem on Dec 26, 2007. Male patient, 41 years of age, was diagnosed with onychomycosis and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . LAMISIL dosage: unknown. Patient recovered.
Pepcid Side Effects Report #5581021-2
PEPCID problem was reported by a Pharmacist from JAPAN on Dec 28, 2007. Female patient, 85 years of age, was treated with PEPCID. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . PEPCID dosage: unknown. During the same period patient was treated with STARSIS, AMLODIN, MUCOSTA, GLAKAY, ROCALTROL, FLOMOX. Patient recovered.
Monurol Side Effects Report #5584633-5
Consumer or non-health professional from FRANCE reported MONUROL problem on Dec 20, 2007. Female patient, 94 years of age, weighting 154.3 lb, was treated with MONUROL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, bundle branch block left, renal failure, . MONUROL dosage: 3 MG PO. During the same period patient was treated with IRBESARTAN, INDAPAMIDE, IPERTEN, TEMERIT, LASLILIX, MEDIATENSYL, NITROGLYCERIN, PLAVIX. Patient was hospitalized. Patient recovered.
Ambisome Side Effects Report #5584680-3
AMBISOME problem was reported by a Health Professional from FRANCE on Dec 18, 2007. Female patient, 58 years of age, was diagnosed with lung disorder and was treated with AMBISOME. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, cardiac arrest, respiratory arrest, . AMBISOME dosage: unknown. During the same period patient was treated with HERCEPTIN, ARIMIDEX, PERINDOPRIL ERBUMINE, ATARAX, HYDROCORTISONE, VFEND, CIFLOX, IMIPENEM AND CILASTATIN. Patient was hospitalized. Patient recovered.
Lisinopril Side Effects Report #5585455-1
Pharmacist from UNITED STATES reported LISINOPRIL problem on Jan 04, 2008. Female patient, weighting 273.2 lb, was diagnosed with hypertension, hypokalaemia and was treated with LISINOPRIL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, hypokalaemia, . LISINOPRIL dosage: unknown. During the same period patient was treated with IRBESARTAN, ASPIRIN, FUROSEMIDE, FLUVASTATIN, CARVEDILOL, SYNTHROID, GLIMEPIRIDE. Patient was hospitalized. Patient recovered.
Tamoxifen Side Effects Report #5586150-5
TAMOXIFEN MERCK NM problem was reported by a Health Professional from SWEDEN on Dec 20, 2007. Female patient was diagnosed with breast cancer and was treated with TAMOXIFEN MERCK NM. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . TAMOXIFEN MERCK NM dosage: 20 MG; ORAL. Patient recovered.
Vesicare Side Effects Report #5587127-6
Physician from JAPAN reported VESICARE problem on Dec 27, 2007. Female patient, 72 years of age, was treated with VESICARE. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . VESICARE dosage: unknown. During the same period patient was treated with MAGNESIUM OXIDE. Patient recovered.
Metformin Side Effects Report #5592668-1
METFORMIN HYDROCHLORIDE problem was reported by a Physician from UNITED STATES on Jan 03, 2008. Male patient, 41 years of age, was diagnosed with type 2 diabetes mellitus and was treated with METFORMIN HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, blood pressure diastolic decreased, bradycardia, cardiac arrest, confusional state, dehydration, diarrhoea, haemodialysis, lethargy, . METFORMIN HYDROCHLORIDE dosage: 1000 MG; BID;. During the same period patient was treated with FOSINOPRIL. Patient was hospitalized. Patient recovered.
Starsis Side Effects Report #5597132-1
Pharmacist from JAPAN reported STARSIS problem on Jan 11, 2008. Female patient, 85 years of age, was diagnosed with diabetes mellitus and was treated with STARSIS. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . STARSIS dosage: unknown. During the same period patient was treated with GASTER, MUCOSTA, GLAKAY, ROCALTROL, FLOMOX. Patient recovered.
Temodal Side Effects Report #5603302-6
TEMODAL problem was reported by a Physician from GERMANY on Jan 15, 2008. Female patient, 68 years of age, weighting 123.5 lb, was diagnosed with glioblastoma and was treated with TEMODAL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, cerebral haemorrhage, coma, haematocrit decreased, haemoglobin decreased, mean cell haemoglobin increased, mean cell volume increased, red blood cell count decreased, vomiting, . TEMODAL dosage: 200 MG; QD; PO. During the same period patient was treated with CITALOPRAM HYDROBROMIDE. Patient was hospitalized. Patient died on 01/09/2008.
Lisinopril Side Effects Report #5605907-5
Pharmacist from UNITED STATES reported LISINOPRIL problem on Jan 24, 2008. Male patient, 63 years of age, weighting 230.4 lb, was diagnosed with hypertension and was treated with LISINOPRIL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . LISINOPRIL dosage: 20MG BID PO. Patient recovered.
Cilostazol Side Effects Report #5606081-1
CILOSTAZOL problem was reported by a Consumer or non-health professional from GERMANY on Jan 09, 2008. Male patient, 66 years of age, was diagnosed with intermittent claudication and was treated with CILOSTAZOL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, bronchitis, chronic obstructive pulmonary disease, condition aggravated, dyspnoea, headache, leukocytosis, sinus tachycardia, . CILOSTAZOL dosage: 200 MG ORAL. During the same period patient was treated with THEOPHYLLINE, NEBIVOLOL, DIGITOXIN, ASPIRIN, SIMVASTATIN. Patient was hospitalized. Patient recovered.
Letairis Side Effects Report #5608215-1
Health Professional from UNITED STATES reported LETAIRIS problem on Jan 22, 2008. Female patient, weighting 148.1 lb, was diagnosed with pulmonary hypertension, essential hypertension, hypercholesterolaemia and was treated with LETAIRIS. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . LETAIRIS dosage: unknown. During the same period patient was treated with REVATIO, SPIRONOLACTONE, COUMADIN, TOPROL, CARTIA XT, GEMFIBROZIL, ZOCOR, PREMARIN. Patient recovered.
Gabapen Side Effects Report #5609839-8
GABAPEN problem was reported by a Physician from JAPAN on Jan 21, 2008. Male patient, 37 years of age, was diagnosed with epilepsy and was treated with GABAPEN. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, pancreatitis acute, peritonitis, . GABAPEN dosage: unknown. During the same period patient was treated with ALEVIATIN. Patient was hospitalized. Patient recovered.
Byetta Side Effects Report #5649193-9
Consumer or non-health professional from UNITED STATES reported BYETTA problem on Oct 26, 2007. Male patient, 84 years of age, weighting 242.1 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 increased, diarrhoea, dyspnoea, renal failure, stomach discomfort, urinary tract infection, . BYETTA dosage: unknown. During the same period patient was treated with NOVOLOG, LOPRESSOR, LISINOPRIL, LASIX. Patient was hospitalized. Patient recovered.
Potassium Side Effects Report #5535765-9
POTASSIUM CHLORIDE problem was reported by a Pharmacist from UNITED STATES on Dec 03, 2007. Male patient, 79 years of age, was diagnosed with mineral supplementation and was treated with POTASSIUM CHLORIDE. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, confusional state, . POTASSIUM CHLORIDE dosage: unknown. Patient was hospitalized. Patient recovered.
Digoxin Side Effects Report #5545318-4
Pharmacist from UNITED STATES reported DIGOXIN problem on Dec 05, 2007. Female patient, 84 years of age, was diagnosed with oedema peripheral and was treated with DIGOXIN. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, bradycardia, fall, international normalised ratio increased, renal failure acute, therapeutic agent toxicity, . DIGOXIN dosage: 0.25MG DAILY PO. During the same period patient was treated with LISINOPRIL, WARFARIN, ALPRAZOLAM, AMITRIPTLINE, DILTIAZEM, AMBIEN CR, ASPIRIN, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.
Narcan Side Effects Report #5546336-2
NARCAN problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 06, 2007. Male patient, 49 years of age, weighting 185.0 lb, was diagnosed with po2 decreased and was treated with NARCAN. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, blood pressure decreased, conversion disorder, convulsion, crying, diarrhoea, diverticulitis, feeling hot, . NARCAN dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.
Valsartan Side Effects Report #5556105-5
Health Professional from KOREA, REPUBLIC OF reported VALSARTAN problem on Dec 03, 2007. Female patient, 75 years of age, was diagnosed with hypertension and was treated with VALSARTAN. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, bradycardia, left ventricular failure, . VALSARTAN dosage: 80 MG, UNK. During the same period patient was treated with TENORMIN. Patient recovered.
Amaryl Side Effects Report #5557228-7
AMARYL problem was reported by a Consumer or non-health professional from on Dec 07, 2007. Male patient, 70 years of age, was diagnosed with hypertension and was treated with AMARYL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . AMARYL dosage: unknown. During the same period patient was treated with DIOVAN, NORVASC. Patient recovered.
Olmesartan Side Effects Report #5564790-7
Consumer or non-health professional from JAPAN reported OLMESARTAN MEDOXOMIL problem on Nov 30, 2007. Male patient was treated with OLMESARTAN MEDOXOMIL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, renal impairment, . OLMESARTAN MEDOXOMIL dosage: 20 MG, PER ORAL. Patient recovered.
Lamisil Side Effects Report #5565934-3
LAMISIL problem was reported by a Physician from JAPAN on Dec 11, 2007. Male patient, 41 years of age, was diagnosed with nail tinea and was treated with LAMISIL. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, . LAMISIL dosage: unknown. Patient recovered.
Diclofenac Side Effects Report #5572383-0
Physician from UNITED KINGDOM reported DICLOFENAC DELAYED problem on Dec 05, 2007. Female patient, 13 years of age, was diagnosed with analgesia and was treated with DICLOFENAC DELAYED. After drug was administered, patient experienced the following problems/side effects: blood potassium increased, haemodialysis, haemoglobin decreased, haemorrhagic infarction, renal impairment, renal tubular necrosis, . DICLOFENAC DELAYED dosage: 50 MG;RECT. During the same period patient was treated with HYDROCORTISONE, MESALAMINE, CEFOTAXIME, METRONIDAZOLE. Patient was hospitalized. Patient recovered.