BLOOD POTASSIUM DECREASED side effect
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Drugs associated with BLOOD POTASSIUM DECREASED
ABILIFY ACCUTANE ACETAMINOPHEN ADENOSCAN ADVAIR ALEVE ALKERAN ALPRAZOLAM ALTACE AMANTADINE AMBISOME AMEVIVE AMIODARONE AMITIZA AMITRIPTYLINE AMLODIPINE ARAVA ARICEPT ARIMIDEX ASMANEX ATIVAN AVANDIA AVASTIN AVELOX AVODART AVONEX BENADRYL BENICAR BETASERON BEVACIZUMAB BONIVA BRONKAID BUMETANIDE BUSPAR BUSULFAN BUSULFEX BYETTA CALCIUM CAMPATH CAMPTO CAP CAPECITABINE CARBAMAZEPINE CARBOPLATIN CEFAZOLIN CELEBREX CELEXA CEREZYME CETUXIMAB CHANTIX CIPRO CISPLATIN CITALOPRAM CLOFARABINE CLOLAR CLOMIPHENE COMMIT COMPAZINE CONCERTA CONCOR COPAXONE COREG COSMEGEN COUMADIN CRESTOR CVS CYCLOPHOSPHAMIDE CYMBALTA CYTARABINE DASATINIB DEPAKOTE DETROL DIANEAL DIGITEK DIGOXIN DILTIAZEM DIOVAN DOCETAXEL DONEPEZIL DORYX DOXORUBICIN DURAGESIC EMTRICITABINE ENBREL ENDOXAN ENULOSE EPIRUBICIN EPIVIR ERBITUX ERLOTINIB ERYTHROMYCIN ESCITALOPRAM ETHYOL EXELON EXENATIDE EXJADE EXUBERA FABRAZYME FASLODEX FENTANYL FLUCONAZOLE FLUOROURACIL FLUOXETINE FORASEQ FORTEO FUROSEMIDE GABITRIL GEMCITABINE GEMZAR GEODON GINGER GLEEVEC HALOPERIDOL HEPARIN HERBESSER HIGROTON HUMALOG HUMATROPE HUMIRA HYDROCHLOROTHIAZ HYDRODIURIL HYZAAR IBUPROFEN IDURSULFASE IMATINIB INDERAL INFERGEN INTERFERON INVEGA IRESSA ISONIAZID ITRACONAZOLE ITRIZOLE JANUVIA KENALOG LACTULOSE LAMICTAL LANTUS LAPATINIB LAPATINIBLET LASIX LETAIRIS LETROZOLE LEUKINE LEVAQUIN LEXAPRO LIPITOR LISINOPRIL LITHIUM LOPRESSOR LORAZEPAM LOTREL LOVASTATIN LOVENOX LUNESTA LYRICA LYSODREN MAVIK MAXZIDE MELPHALAN MEMANTINE METAMUCIL METFORMIN METHADONE METHYLIN MICARDIS MIDOL MILK MIRALAX MIRENA MITOXANGTRONE MOBIC MOPRAL MOVIPREP MUCINEX MYLAN MYLOTARG NAFCILLIN NAGLAZYME NAMENDA NATALIZUMAB NEUPOGEN NEXAVAR NEXIUM NICOTINE NORVASC NOVOLOG NOVOSEVEN ORLISTAT ORTHO OSMOPREP OVIDE OXALIPLATIN OXCARBAZEPINE PACERONE PACLITAXEL PANITUMUMAB PAROXETINE PAXIL PEGASYS PEGETRON PEGINTERFERON PEMETREXED PHOSPHOSODA PIOGLITAZONE PLAVIX POSACONAZOLE POTASSIUM PREDNISOLONE PREDNISONE PRINIVIL PROCHLORPERAZINE PROMETHAZINE PROPECIA PROPYLTHIOURACIL PROVIGIL PROZAC PULMICORT QUESTRAN RANEXA RASILEZ REBIF RECLAST REGLAN REMICADE RETEPLASE REVLIMID RIBASPHERE RIBAVIRIN RISPERDAL RITALIN RITUXAN RITUXIMAB SEROQUEL SERTRALINE SORAFENIB SOTALOL SPIRIVA SPIRONOLACTONE SPIRONOLACTONELE STALEVO SUTENT SYMBICORT SYMLIN SYNTHROID TAB TARCEVA TAVOR TAXOL TAXOTERE TEGRETOL TEKTURNA TEMODAL TEMODAR TEMOZOLOIDE TEMOZOLOMIDE THALIDOMIDE THALOMID TIKOSYN TIOTROPIUM TOPAMAX TOPOTECAN TOPROL TRACLEER TRAMADOL TRASTUZUMAB TRASYLOL TRIAMTERENE TRICILEST TRISENOX TYGACIL TYKERB TYSABRI UNASYN VALTREX VELCADE VENLAFAXINE VERAPAMIL VIAGRA VINCRISTINE VIOKASE VISICOL WARFARIN WELCHOL WINRHO XANAX XELODA XOPENEX XYREM YASMIN ZELNORM ZENAPAX ZOLINZA ZOMETA ZYPREXA ZYVOXTemozolomide Side Effects Report #5648538-3
Consumer or non-health professional from UNITED STATES reported TEMOZOLOMIDE problem on Mar 03, 2008. Female patient, weighting 121.9 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, dehydration, gastroenteritis viral, hypomagnesaemia, hyponatraemia, hypotension, lymphopenia, renal failure acute, . TEMOZOLOMIDE dosage: 5060 MG. Patient was hospitalized. Patient recovered.
Temodar Side Effects Report #5650057-5
TEMODAR problem was reported by a Health Professional from UNITED STATES on Feb 19, 2008. Female patient, 57 years of age, was diagnosed with gliosarcoma and was treated with TEMODAR. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, blood pressure inadequately controlled, brain scan abnormal, contusion, epistaxis, fall, haematemesis, haemorrhage intracranial, hemiparesis, . TEMODAR dosage: 125 MG; QD; PO; 300 MG;. During the same period patient was treated with DECADRON, LEXAPRO, PHENYTOIN. Patient was hospitalized and became disabled. Patient died on 01/06/2008.
Pegetron Side Effects Report #5652233-4
Health Professional from CANADA reported PEGETRON problem on Feb 25, 2008. Female patient, 48 years of age, was diagnosed with hepatitis c and was treated with PEGETRON. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, . PEGETRON dosage: unknown. Patient recovered.
Rebif Side Effects Report #5654410-5
REBIF problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2008. Female patient, 48 years of age, weighting 156.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, convulsion, head banging, tongue biting, . REBIF dosage: unknown. During the same period patient was treated with AMANTADINE, EFFEXOR, BACLOFEN. Patient was hospitalized. Patient recovered.
Amantadine Side Effects Report #5654426-9
Physician from UNITED STATES reported AMANTADINE HYDROCHLORIDE problem on Feb 27, 2008. Female patient, 30 years of age, was diagnosed with pain and was treated with AMANTADINE HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, deep vein thrombosis, disseminated intravascular coagulation, ecchymosis, electrocardiogram qt prolonged, fall, haemodynamic instability, intentional overdose, . AMANTADINE HYDROCHLORIDE dosage: 100 MG, OER ORAL. During the same period patient was treated with ZIPRASIDONE, IBUPROFEN. Patient was hospitalized. Patient died on 01/01/2007.
Topamax Side Effects Report #5654705-5
TOPAMAX problem was reported by a Physician from UNITED STATES on Feb 25, 2008. Male patient, weighting 152.0 lb, was diagnosed with alcohol abuse, hiccups and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, confusional state, dysarthria, facial paresis, gait disturbance, hypertension, speech disorder, . TOPAMAX dosage: unknown. During the same period patient was treated with THORAZINE. Patient recovered.
Docetaxel Side Effects Report #5655497-6
Health Professional from UNITED STATES reported DOCETAXEL problem on Mar 04, 2008. Female patient, 61 years of age, weighting 172.0 lb, was diagnosed with breast cancer and was treated with DOCETAXEL. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, dehydration, vision blurred, . DOCETAXEL dosage: unknown. During the same period patient was treated with CYTOXAN. Patient was hospitalized. Patient recovered.
Oxaliplatin Side Effects Report #5656628-4
OXALIPLATIN problem was reported by a Health Professional from UNITED STATES on Mar 07, 2008. Male patient, weighting 154.0 lb, was diagnosed with laryngeal cancer and was treated with OXALIPLATIN. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, inguinal hernia, obstructive, . OXALIPLATIN dosage: 155MG DAYS 1 + 15Q28DAYS IV DRIP. During the same period patient was treated with XELODA. Patient was hospitalized. Patient recovered.
Tekturna Side Effects Report #5657913-2
Physician from UNITED STATES reported TEKTURNA HCT problem on Mar 03, 2008. Female patient was treated with TEKTURNA HCT. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, weight decreased, . TEKTURNA HCT dosage: unknown. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5658101-6
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 25, 2008. Female patient, 58 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 decreased, dehydration, influenza, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Tekturna Side Effects Report #5659458-2
Physician from UNITED STATES reported TEKTURNA HCT problem on Mar 06, 2008. Female patient, 68 years of age, was treated with TEKTURNA HCT. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, hyponatraemia, weight decreased, . TEKTURNA HCT dosage: 300/12.5MG, QD. During the same period patient was treated with TEKTURNA HCT. Patient was hospitalized. Patient recovered.
Amevive Side Effects Report #5663776-1
AMEVIVE problem was reported by a Physician from UNITED STATES on Feb 29, 2008. Female patient, 79 years of age, was diagnosed with psoriasis and was treated with AMEVIVE. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, cardiac failure congestive, condition aggravated, enterobacter infection, fistula discharge, hypotension, post procedural fistula, post procedural haematoma, retroperitoneal haemorrhage, . AMEVIVE dosage: 15 MG, WEEKLY, INTRAMUSCULAR. During the same period patient was treated with VANCOMYCIN, PROTONIX, LASIX, SYNTHROID, COZAAR, OXYCONTIN, VICODIN, AMBIEN. Patient was hospitalized. Patient recovered.
Thalomid Side Effects Report #5664760-4
Physician from UNITED STATES reported THALOMID problem on Mar 03, 2008. Male patient, 64 years of age, was diagnosed with multiple myeloma and was treated with THALOMID. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, clostridial infection, diarrhoea, herpes zoster, post herpetic neuralgia, renal failure acute, urinary retention, . THALOMID dosage: 100 MG, EVERY EVENING, ORAL; 200 MG, EVERY EVENING, ORAL; 50 MG, 1 IN 1 D, ORAL. During the same period patient was treated with VELCADE, DEXAMETHASONE, MELPHALAN, CISPLATIN. Patient was hospitalized. Patient recovered.
Doryx Side Effects Report #5670357-2
DORYX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 04, 2008. Female patient, 63 years of age, was diagnosed with multiple sclerosis and was treated with DORYX. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, cardiac murmur, dehydration, dizziness, dyspnoea, fall, loss of consciousness, malaise, panic attack, . DORYX dosage: unknown. During the same period patient was treated with COPAXONE. Patient was hospitalized. Patient recovered.
Tekturna Side Effects Report #5670720-X
Physician from UNITED STATES reported TEKTURNA HCT problem on Mar 13, 2008. Female patient, 68 years of age, was treated with TEKTURNA HCT. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, hyponatraemia, weight decreased, . TEKTURNA HCT dosage: 300/12.5MG, QD. During the same period patient was treated with TEKTURNA HCT. Patient was hospitalized. Patient recovered.
Chantix Side Effects Report #5671261-6
CHANTIX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 06, 2008. Female patient, weighting 100.1 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, lung transplant, pulmonary fibrosis, stress, vomiting, . CHANTIX dosage: unknown. During the same period patient was treated with KLONOPIN, NEURONTIN, RISPERDAL, BACLOFEN, REGLAN, TOPROL, PIROXICAM, ORAMORPH. Patient recovered.
Avonex Side Effects Report #5671821-2
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Mar 06, 2008. Female patient, 28 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 decreased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5671828-5
AVONEX problem was reported by a Health Professional from UNITED STATES on Mar 04, 2008. Female patient, 65 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 decreased, nephrolithiasis, sepsis, urinary tract infection, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Dasatinib Side Effects Report #5674829-6
Health Professional from UNITED STATES reported DASATINIB problem on Mar 19, 2008. Female patient, 60 years of age, weighting 136.0 lb, was diagnosed with breast cancer metastatic and was treated with DASATINIB. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, loss of consciousness, . DASATINIB dosage: 50MG BID PO. Patient was hospitalized. Patient recovered.
Heparin Side Effects Report #5677113-X
HEPARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 24, 2008. Female patient, 80 years of age, weighting 114.0 lb, was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, blood potassium increased, coagulopathy, dialysis, platelet count decreased, renal failure, white blood cell count increased, . HEPARIN dosage: unknown. Patient was hospitalized. Patient recovered.
Midol Side Effects Report #5679162-4
Consumer or non-health professional from UNITED STATES reported MIDOL MENSTRUAL COMPLETE MAXIMUM STRENGTH problem on Mar 12, 2008. Female patient, 15 years of age, weighting 125.7 lb, was diagnosed with intentional overdose and was treated with MIDOL MENSTRUAL COMPLETE MAXIMUM STRENGTH. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, somnolence, vomiting, . MIDOL MENSTRUAL COMPLETE MAXIMUM STRENGTH dosage: unknown. Patient recovered.
Avonex Side Effects Report #5680961-3
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 14, 2008. Female patient, 56 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 decreased, blood pressure increased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Rebif Side Effects Report #5689708-8
Health Professional from UNITED STATES reported REBIF problem on Mar 20, 2008. Female patient, 43 years of age, weighting 200.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, chest pain, dyspnoea, pulmonary fibrosis, . REBIF dosage: unknown. During the same period patient was treated with ZOLOFT, BACLOFEN, NEURONTIN, ZANAFLEX, SYNTHROID, AMITRIPTYLINE. Patient was hospitalized. Patient recovered.
Midol Side Effects Report #5610916-6
MIDOL MENSTRUAL COMPLETE MAXIMUM STRENGTH problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 18, 2008. Female patient, 15 years of age, weighting 125.7 lb, was diagnosed with intentional overdose and was treated with MIDOL MENSTRUAL COMPLETE MAXIMUM STRENGTH. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, somnolence, vomiting, . MIDOL MENSTRUAL COMPLETE MAXIMUM STRENGTH dosage: unknown. Patient recovered.
Leukine Side Effects Report #5611999-X
Health Professional from UNITED STATES reported LEUKINE problem on Jan 11, 2008. Female patient, 64 years of age, weighting 90.39 lb, was diagnosed with ovarian cancer metastatic and was treated with LEUKINE. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, . LEUKINE dosage: unknown. During the same period patient was treated with ABRAXANE. Patient recovered.
Cyclophosphamide Side Effects Report #5612669-4
CYCLOPHOSPHAMIDE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 01, 2008. Female patient, weighting 174.2 lb, was treated with CYCLOPHOSPHAMIDE. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, . CYCLOPHOSPHAMIDE dosage: 1313 MG. During the same period patient was treated with DOXORUBICIN HYDROCHLORIDE, ETOPOSIDE, PREDNISONE, RITUXIMAB, VINCRISTINE SULPHATE. Patient recovered.
Trastuzumab Side Effects Report #5614458-3
Physician from UNITED KINGDOM reported TRASTUZUMAB problem on Jan 21, 2008. Female patient was diagnosed with breast cancer metastatic and was treated with TRASTUZUMAB. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, blood urea increased, bone pain, dehydration, fatigue, guillain-barre syndrome, hypotension, lethargy, . TRASTUZUMAB dosage: 4 MG/KG, 1/WEEK. During the same period patient was treated with PACLITAXEL, LAPATINIB, HYDROCHLOROTHIAZIDE, LOPERAMIDE HYDROCHLORIDE, PERCOCET, TELMISARTAN, TEMAZEPAM, ZOLEDRONIC ACID. Patient was hospitalized. Patient recovered.
Temozolomide Side Effects Report #5614935-5
TEMOZOLOMIDE problem was reported by a Pharmacist from UNITED STATES on Feb 04, 2008. Female patient, 57 years of age, weighting 141.0 lb, was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, blood pressure increased, confusional state, contusion, epistaxis, fall, haematemesis, haemorrhage intracranial, headache, . TEMOZOLOMIDE dosage: 300 MG 5X PER MONTH PO. Patient was hospitalized. Patient died on 01/06/2008.
Cosmegen Side Effects Report #5615740-6
Consumer or non-health professional from UNITED STATES reported COSMEGEN problem on Jan 22, 2008. Male patient, 32 years of age, was diagnosed with germ cell cancer and was treated with COSMEGEN. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, febrile neutropenia, haemoglobin decreased, neutropenic sepsis, platelet count decreased, . COSMEGEN dosage: 1.6 MG/M**2; Q2W; IV. During the same period patient was treated with CISPLATIN, ETOPOSIDE, METHOTREXATE, ACETAZOLAMIDE, DEXTROSE WITH POTASSIUM BICARBONATE AND S, FILGRASTIM, FOLINIC ACID. Patient died on 05/07/2001.
Leukine Side Effects Report #5620601-2
LEUKINE problem was reported by a Health Professional from UNITED STATES on Jan 29, 2008. Female patient, 64 years of age, weighting 90.39 lb, was diagnosed with ovarian cancer metastatic and was treated with LEUKINE. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, headache, nausea, ovarian cancer metastatic, vomiting, . LEUKINE dosage: unknown. During the same period patient was treated with ABRAXANE. Patient died on 01/19/2008.
Topamax Side Effects Report #5621298-8
Physician from UNITED STATES reported TOPAMAX problem on Jan 30, 2008. Male patient, weighting 152.0 lb, was diagnosed with alcohol abuse and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, confusional state, dysarthria, facial paresis, gait disturbance, hypertension, speech disorder, . TOPAMAX dosage: unknown. Patient recovered.
Rasilez Side Effects Report #5623078-6
RASILEZ problem was reported by a Physician from GERMANY on Feb 07, 2008. Female patient was treated with RASILEZ. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, . RASILEZ dosage: 150 MG, QD. Patient recovered.
Rebif Side Effects Report #5625435-0
Consumer or non-health professional from UNITED STATES reported REBIF problem on Jan 28, 2008. Female patient, 55 years of age, weighting 170.0 lb, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, condition aggravated, dehydration, depression, ear infection, gastroenteritis viral, liver function test abnormal, lymphadenopathy, red blood cell count decreased, . REBIF dosage: unknown. During the same period patient was treated with TYLENOL, REGLAN, EFFEXOR, NORVASC, DIOVAN, PHENERGAN, LORAZEPAM, FOSAMAX. Patient was hospitalized. Patient recovered.
Avonex Side Effects Report #5628842-5
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 30, 2008. Female patient, 43 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 decreased, neck pain, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Symlin Side Effects Report #5628931-5
Consumer or non-health professional from UNITED STATES reported SYMLIN problem on Feb 01, 2008. Female patient, 54 years of age, weighting 240.0 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 decreased, hypoglycaemia, tremor, . SYMLIN dosage: unknown. During the same period patient was treated with LANTUS, DIOVAN, HYDROCHLOROTHIAZIDE, MONOPRIL, TOPROL. Patient recovered.
Avonex Side Effects Report #5628994-7
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 30, 2008. 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 decreased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Exjade Side Effects Report #5629912-8
Physician from FRANCE reported EXJADE problem on Feb 07, 2008. Female patient, child 6 years of age, weighting 46.30 lb, was diagnosed with thalassaemia beta and was treated with EXJADE. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, glycosuria, microalbuminuria, renal tubular disorder, urine potassium increased, urine sodium increased, . EXJADE dosage: 500 MG/DAY. Patient recovered.
Phosphosoda Side Effects Report #5630638-5
PHOSPHOSODA GINGER LEMON problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 28, 2008. Female patient, 56 years of age, was diagnosed with endoscopy gastrointestinal and was treated with PHOSPHOSODA GINGER LEMON. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, cold sweat, dizziness, gastric disorder, nausea, retching, tremor, . PHOSPHOSODA GINGER LEMON dosage: 45 ML; X1; PO. During the same period patient was treated with ACTOS, METOPROLOL TARTRATE, PRILOSEC. Patient recovered.
Cymbalta Side Effects Report #5633455-5
Physician from UNITED STATES reported CYMBALTA problem on Feb 13, 2008. Female patient, 55 years of age, was treated with CYMBALTA. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, . CYMBALTA dosage: unknown. During the same period patient was treated with METHADONE, NORCO, PRILOSEC, LISINOPRIL. Patient was hospitalized. Patient recovered.
Amevive Side Effects Report #5643945-7
AMEVIVE problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 15, 2008. Female patient, 79 years of age, was diagnosed with psoriasis and was treated with AMEVIVE. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, cardiac failure congestive, condition aggravated, enterobacter infection, hypotension, post procedural haematoma, retroperitoneal haematoma, retroperitoneal haemorrhage, staphylococcal infection, . AMEVIVE dosage: 15 MG, WEEKLY, INTRAMUSCULAR. During the same period patient was treated with VANCOMYCIN, PROTONIX, LASIX, SYNTHROID, COZAAR, OXYCONTIN, VICODIN, AMBIEN. Patient was hospitalized. Patient recovered.
Reglan Side Effects Report #5644398-5
Consumer or non-health professional from UNITED STATES reported REGLAN problem on Feb 11, 2008. Female patient, 74 years of age, weighting 122.0 lb, was diagnosed with impaired gastric emptying and was treated with REGLAN. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, blood sodium decreased, dry eye, dry mouth, fall, insomnia, malaise, malnutrition, . REGLAN dosage: unknown. During the same period patient was treated with HYDROCHLOROTHIAZIDE, NORVASC, SYNTHROID, PEPCID, PRAVACHOL, BENICAR. Patient was hospitalized and became disabled. Patient recovered.
Fentanyl Side Effects Report #5645182-9
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 20, 2008. Female patient, weighting 150.0 lb, was diagnosed with impaired gastric emptying, depression, migraine, restless legs syndrome, anxiety and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, mental disorder, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with ESTRACE, LEXAPRO, TOPAMAX, ZANAFLEX, KLONOPIN. Patient was hospitalized. Patient recovered.
Carboplatin Side Effects Report #5647168-7
Consumer or non-health professional from UNITED STATES reported CARBOPLATIN problem on Feb 28, 2008. Male patient, weighting 144.4 lb, was treated with CARBOPLATIN. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, blood sodium decreased, dehydration, flatulence, intestinal dilatation, intussusception, no therapeutic response, rectal haemorrhage, renal failure acute, . CARBOPLATIN dosage: 92 MG. During the same period patient was treated with TAXOL. Patient was hospitalized. Patient recovered.
Mopral Side Effects Report #5579413-0
MOPRAL problem was reported by a Physician from BELGIUM on Dec 26, 2007. Female patient, weighting 106.5 lb, was treated with MOPRAL. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, confusional state, fatigue, gastrointestinal candidiasis, hypersensitivity, pain, photosensitivity reaction, urticaria, . MOPRAL dosage: unknown. During the same period patient was treated with ESTROGEL, PREDNISOLONE. Patient was hospitalized and became disabled. Patient recovered.
Betaseron Side Effects Report #5581519-7
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Nov 29, 2007. Female patient, 48 years of age, weighting 178.6 lb, was diagnosed with multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, chest pain, diarrhoea, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.
Ibuprofen Side Effects Report #5584001-6
IBUPROFEN problem was reported by a Pharmacist from UNITED STATES on Jan 03, 2008. Female patient, 25 years of age, was diagnosed with caesarean section, procedural pain and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, dehydration, incision site infection, renal failure acute, . IBUPROFEN dosage: 800 MG Q8HRS PO. Patient was hospitalized. Patient recovered.
Acetaminophen Side Effects Report #5584590-1
Health Professional from UNITED KINGDOM reported ACETAMINOPHEN problem on Aug 14, 2007. Female patient was treated with ACETAMINOPHEN. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, overdose, . ACETAMINOPHEN dosage: unknown. Patient was hospitalized. Patient recovered.
Revlimid Side Effects Report #5584878-4
REVLIMID problem was reported by a Physician from UNITED STATES on Dec 27, 2007. Male patient, 53 years of age, weighting 192.0 lb, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, cardiac arrest, chest discomfort, coronary artery disease, hyperhidrosis, loss of consciousness, ventricular fibrillation, . REVLIMID dosage: 10 MG, 1 IN 1 D, ORAL. During the same period patient was treated with ASPIRIN, ZOMETA, DEXAMETHASONE. Patient was hospitalized. Patient recovered.
Ribavirin Side Effects Report #5584913-3
Consumer or non-health professional from UNITED STATES reported RIBAVIRIN problem on Dec 28, 2007. Male patient, 62 years of age, weighting 190.0 lb, was diagnosed with hepatitis c and was treated with RIBAVIRIN. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, dehydration, diarrhoea, weight decreased, white blood cell count decreased, . RIBAVIRIN dosage: unknown. During the same period patient was treated with PEGASYS. Patient was hospitalized. Patient recovered.
Hydrodiuril Side Effects Report #5585608-2
HYDRODIURIL problem was reported by a Physician from UNITED STATES on Dec 31, 2007. Male patient, 64 years of age, was treated with HYDRODIURIL. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, chest pain, . HYDRODIURIL dosage: unknown. During the same period patient was treated with PRINIVIL, ATENOLOL, DOXAZOSIN MESYLATE. Patient was hospitalized. Patient recovered.
Amevive Side Effects Report #5591542-4
Physician from UNITED STATES reported AMEVIVE problem on Jan 03, 2008. Female patient, 79 years of age, was diagnosed with psoriasis and was treated with AMEVIVE. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, cardiac failure congestive, condition aggravated, enterobacter infection, fistula, hypotension, post procedural haematoma, retroperitoneal haemorrhage, wound infection staphylococcal, . AMEVIVE dosage: 15 MG, WEEKLY, INTRAMUSCULAR. During the same period patient was treated with VANCOMYCIN, PROTONIX, LASIX, SYNTHROID, COZAAR, OXYCONTIN, VICODIN, AMBIEN. Patient was hospitalized. Patient recovered.