BLOOD ALKALINE PHOSPHATASE DECREASED side effect
What is BLOOD ALKALINE PHOSPHATASE DECREASED ?
Help Community - Describe Your Side Effect
Search FDA Side Effects
Ask Health Expert
BLOOD ALKALINE PHOSPHATASE DECREASED and Recently Reported Side Effects
BLOOD ALKALINE PHOSPHATASE DECREASED and 15 most Active Side Effect polls
BLOOD ALKALINE PHOSPHATASE DECREASED and featured health surveys
Substances toxic to Health
Recent Hospital reviews
Comments about Side Effects
Hospital Quality reviews
Homecare Quality reviews
Drugs associated with BLOOD ALKALINE PHOSPHATASE DECREASED
ALLOPURINOL ARTIST ASACOL CAMPTOSAR CARVEDILOL CHANTIX COMTAN DIOVAN FORTUM RECLAST REQUIP RIFAMPICIN STRATTERA TEMOZOLOMIDE TYSABRI VELCADE ZIDOVUDINE ZOCORArtist Side Effects Report #5564977-3
Consumer or non-health professional from JAPAN reported ARTIST problem on Dec 07, 2007. Male patient, 35 years of age, was diagnosed with self mutilation and was treated with ARTIST. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, blood lactate dehydrogenase, fibrin increased, overdose, paralysis, shock, suicide attempt, vomiting, white blood cell count increased, . ARTIST dosage: 320MG PER DAY. During the same period patient was treated with ALLOPURINOL, OLMETEC, ADALAT, DIOVAN, SPIRITS. Patient was hospitalized. Patient recovered.
Carvedilol Side Effects Report #5504207-1
CARVEDILOL problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Oct 29, 2007. Male patient, 35 years of age, was diagnosed with self mutilation and was treated with CARVEDILOL. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, blood lactate dehydrogenase increased, fibrin increased, paralysis, shock, suicide attempt, vomiting, white blood cell count increased, . CARVEDILOL dosage: 320MG SINGLE DOSE. During the same period patient was treated with ALLOPURINOL, ADALAT, DIOVAN, OLMETEC, SPIRITS, ACTIVATED CARBON, SORBITOL. Patient was hospitalized. Patient recovered.
Allopurinol Side Effects Report #5514758-1
Health Professional from UNITED KINGDOM reported ALLOPURINOL BP problem on Oct 30, 2007. Female patient was diagnosed with self mutilation and was treated with ALLOPURINOL BP. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, blood lactate dehydrogenase increased, fibrin increased, overdose, paralysis, shock, vomiting, white blood cell count increased, . ALLOPURINOL BP dosage: 3200 MG, UNK. During the same period patient was treated with ADALAT, CARVEDILOLO RANBAXY, DIOVAN, OLMETEC. Patient was hospitalized. Patient recovered.
Artist Side Effects Report #5529378-2
ARTIST problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Nov 26, 2007. Male patient, 35 years of age, was diagnosed with self mutilation and was treated with ARTIST. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, blood lactate dehydrogenase increased, fibrin increased, overdose, paralysis, shock, vomiting, white blood cell count increased, . ARTIST dosage: 320MG PER DAY. During the same period patient was treated with ALLOPURINOL, OLMETEC, ADALAT, DIOVAN, SPIRITS. Patient was hospitalized. Patient recovered.
Carvedilol Side Effects Report #5529380-0
Consumer or non-health professional from UNITED KINGDOM reported CARVEDILOL problem on Nov 26, 2007. Male patient, 35 years of age, was diagnosed with self mutilation and was treated with CARVEDILOL. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, blood lactate dehydrogenase increased, fibrin increased, paralysis, shock, suicide attempt, vomiting, white blood cell count increased, . CARVEDILOL dosage: 320MG SINGLE DOSE. During the same period patient was treated with ALLOPURINOL, ADALAT, DIOVAN, OLMETEC, SPIRITS, ACTIVATED CARBON, SORBITOL. Patient was hospitalized. Patient recovered.
Artist Side Effects Report #5480468-2
ARTIST problem was reported by a Health Professional from UNITED KINGDOM on Oct 05, 2007. Male patient, 35 years of age, was diagnosed with self mutilation and was treated with ARTIST. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, blood lactate dehydrogenase increased, fibrin increased, overdose, paralysis, shock, vomiting, white blood cell count increased, . ARTIST dosage: 320MG PER DAY. During the same period patient was treated with ALLOPURINOL, OLMETEC, ADALAT, DIOVAN. Patient was hospitalized. Patient recovered.
Artist Side Effects Report #5480584-5
Health Professional from UNITED KINGDOM reported ARTIST problem on Oct 05, 2007. Male patient, 35 years of age, was diagnosed with self mutilation and was treated with ARTIST. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, blood lactate dehydrogenase increased, fibrin increased, overdose, paralysis, shock, vomiting, white blood cell count increased, . ARTIST dosage: 320MG PER DAY. During the same period patient was treated with ALLOPURINOL, OLMETEC, ADALAT, DIOVAN. Patient was hospitalized. Patient recovered.
Diovan Side Effects Report #5490471-4
DIOVAN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Oct 16, 2007. Male patient, 35 years of age, was diagnosed with self mutilation and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, blood lactate dehydrogenase increased, fibrin increased, gastrointestinal tube insertion, heart rate decreased, hypotension, overdose, paralysis, respiratory rate decreased, . DIOVAN dosage: 40MGX 8 TABLETS. During the same period patient was treated with ADALAT, ALLOPURINOL, CARVEDILOL, OLMETEC, ALCOHOL. Patient was hospitalized. Patient recovered.
Zidovudine Side Effects Report #5492690-X
Consumer or non-health professional from UNITED STATES reported ZIDOVUDINE problem on Oct 02, 2007. Male patient, 13 years of age, was diagnosed with hiv infection and was treated with ZIDOVUDINE. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, immune reconstitution syndrome, leukopenia, mycobacterium avium complex infection, . ZIDOVUDINE dosage: unknown. During the same period patient was treated with LAMIVUDINE, EFAVIRENZ, LOPINAVIR AND RITONAVIR, AZITHROMYCIN, CLINDAMYCIN. Patient was hospitalized. Patient recovered.
Allopurinol Side Effects Report #5503613-9
ALLOPURINOL problem was reported by a Health Professional from UNITED KINGDOM on Oct 15, 2007. Male patient, 35 years of age, was diagnosed with self mutilation and was treated with ALLOPURINOL. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, blood lactate dehydrogenase increased, fibrin increased, overdose, paralysis, shock, vomiting, white blood cell count increased, . ALLOPURINOL dosage: unknown. During the same period patient was treated with CARVEDILOL, ADALAT, DIOVAN, OLMESARTAN MEDOXOMIL. Patient was hospitalized. Patient recovered.
Fortum Side Effects Report #5384196-3
Physician from FRANCE reported FORTUM problem on July 11, 2007. Female patient, 59 years of age, was diagnosed with pseudomonas infection and was treated with FORTUM. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, monocyte percentage increased, neutropenia, white blood cell count decreased, . FORTUM dosage: unknown. During the same period patient was treated with TAMOXIFEN CITRATE. Patient recovered.
Fortum Side Effects Report #5384196-3
FORTUM problem was reported by a Physician from FRANCE on July 11, 2007. Female patient, 59 years of age, was diagnosed with pseudomonas infection and was treated with FORTUM. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, monocyte percentage increased, neutropenia, white blood cell count decreased, . FORTUM dosage: unknown. During the same period patient was treated with TAMOXIFEN CITRATE. Patient recovered.
Zocor Side Effects Report #5777909-X
Physician from CANADA reported ZOCOR problem on June 16, 2008. Female patient, 57 years of age, was diagnosed with arthritis and was treated with ZOCOR. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, burning sensation, chest pain, confusional state, constipation, dyspnoea, dyspnoea exertional, hypoaesthesia, lacunar infarction, . ZOCOR dosage: unknown. During the same period patient was treated with ADVAIR DISKUS, GLUCOSAMINE, ASPIRIN, VENTOLIN. Patient was hospitalized. Patient recovered.
Zocor Side Effects Report #5699911-9
ZOCOR problem was reported by a Physician from CANADA on Apr 03, 2008. Female patient, 57 years of age, was diagnosed with arthritis and was treated with ZOCOR. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, burning sensation, chest pain, confusional state, constipation, dyspnoea, dyspnoea exertional, hypoaesthesia, lacunar infarction, . ZOCOR dosage: unknown. During the same period patient was treated with ADVAIR HFA, GLUCOSAMINE, ASPIRIN, VENTOLIN. Patient was hospitalized. Patient recovered.
Asacol Side Effects Report #5353176-6
Pharmacist from UNITED STATES reported ASACOL problem on May 25, 2007. Male patient, 22 years of age, weighting 149.9 lb, was diagnosed with crohn's disease and was treated with ASACOL. After drug was administered, patient experienced the following problems/side effects: blood alkaline phosphatase decreased, blood bilirubin increased, blood glucose increased, blood potassium decreased, blood urea increased, brain oedema, head injury, hemiparesis, subdural haematoma, . ASACOL dosage: unknown. Patient was hospitalized. Patient recovered.
Chantix Side Effects Report #5475237-3
CHANTIX problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 20, 2007. Female patient, weighting 119.9 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: abnormal dreams, blood alkaline phosphatase decreased, blood glucose increased, blood potassium decreased, constipation, flatulence, nausea, personality change, psychotic disorder, . CHANTIX dosage: unknown. During the same period patient was treated with VALIUM. Patient was hospitalized. Patient recovered.
Reclast Side Effects Report #5494991-8
Physician from UNITED STATES reported RECLAST problem on Oct 18, 2007. Male patient, 81 years of age, weighting 153.0 lb, was diagnosed with osteitis deformans and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: asthenia, blood alkaline phosphatase decreased, blood creatine phosphokinase increased, chills, confusional state, diastolic dysfunction, dizziness, dyspnoea, electrocardiogram t wave abnormal, . RECLAST dosage: 5 MG ONCE. During the same period patient was treated with ALTACE, LIPITOR, ASACOL, ASCORBIC ACID, ASPIRIN, FLEMEX. Patient was hospitalized. Patient recovered.
Reclast Side Effects Report #5500947-9
RECLAST problem was reported by a Physician from UNITED STATES on Oct 24, 2007. Male patient, 81 years of age, weighting 153.0 lb, was diagnosed with osteitis deformans and was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: asthenia, blood alkaline phosphatase decreased, blood creatine phosphokinase increased, chills, confusional state, diastolic dysfunction, dizziness, dyspnoea, electrocardiogram t wave abnormal, . RECLAST dosage: 5 MG ONCE. During the same period patient was treated with ALTACE, LIPITOR, ASACOL, ASCORBIC ACID, ASPIRIN, FLEMEX. Patient was hospitalized. Patient recovered.
Camptosar Side Effects Report #5443368-X
Consumer or non-health professional from UNITED STATES reported CAMPTOSAR problem on Aug 31, 2007. Male patient, weighting 29.32 lb, was treated with CAMPTOSAR. After drug was administered, patient experienced the following problems/side effects: back pain, blood alkaline phosphatase decreased, incorrect dose administered, neuroblastoma, protein total decreased, . CAMPTOSAR dosage: 295 MG. During the same period patient was treated with TEMOZOLOMIDE. Patient recovered.
Temozolomide Side Effects Report #5768564-3
TEMOZOLOMIDE problem was reported by a Physician from ISRAEL on June 03, 2008. Male patient, 67 years of age, weighting 125.7 lb, was diagnosed with glioblastoma multiforme and was treated with TEMOZOLOMIDE. After drug was administered, patient experienced the following problems/side effects: balance disorder, blood alkaline phosphatase decreased, blood cholesterol increased, blood glucose increased, blood phosphorus decreased, depressed level of consciousness, fall, fatigue, haematocrit increased, . TEMOZOLOMIDE dosage: 130 MG;QD;PO. During the same period patient was treated with AUGMENTIN, DEXAMETHASONE, HEPARIN, BROTIZOLAM. Patient was hospitalized. Patient recovered.
Velcade Side Effects Report #5376669-4
Physician from JAPAN reported VELCADE problem on June 18, 2007. Male patient, 71 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: aspergillosis, blood alkaline phosphatase decreased, blood glucose increased, blood lactate dehydrogenase increased, blood urea increased, blood uric acid increased, c-reactive protein increased, congestive cardiomyopathy, febrile neutropenia, . VELCADE dosage: 1.00 MG/M2, INTRAVENOUS. During the same period patient was treated with ZOMETA, BICARBONATE, NEUTROGIN, AMIKACIN SULPHATE, LASIX, VORICONAZOLE, RABEPRAZOLE, ENALAPRIL MALEATE. Patient died on 05/07/2007.
Velcade Side Effects Report #5332903-8
VELCADE problem was reported by a Physician from JAPAN on May 08, 2007. Male patient, 71 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: basophil count decreased, blood alkaline phosphatase decreased, blood glucose increased, blood lactate dehydrogenase increased, blood urea increased, blood uric acid increased, computerised tomogram thorax abnormal, condition aggravated, febrile neutropenia, . VELCADE dosage: 1.00 MG/M2, INTRAVENOUS. During the same period patient was treated with ZOMETA, BICARBONATE, NEUTROGIN, AMIKACIN SULPHATE, LASIX, VORICONAZOLE, RABEPRAZOLE, ENALAPRIL MALEATE. Patient died on 05/07/2007.
Rifampicin Side Effects Report #5338799-2
Physician from BRAZIL reported RIFAMPICIN problem on May 18, 2007. Female patient, 37 years of age, weighting 138.9 lb, was diagnosed with leprosy and was treated with RIFAMPICIN. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, blood alkaline phosphatase decreased, blood bilirubin abnormal, blood glucose decreased, blood sodium decreased, cyanosis, discomfort, fatigue, . RIFAMPICIN dosage: unknown. During the same period patient was treated with DAPSONE, CLOFAZIMINE. Patient recovered.
Velcade Side Effects Report #5341862-3
VELCADE problem was reported by a Physician from JAPAN on May 16, 2007. Male patient, 71 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: basophil count decreased, blood alkaline phosphatase decreased, blood glucose increased, blood immunoglobulin g increased, blood lactate dehydrogenase increased, blood urea decreased, blood urea increased, blood uric acid increased, c-reactive protein increased, . VELCADE dosage: 1.00 MG/M2, UNK, INTRAVENOUS. During the same period patient was treated with ZOMETA, BICARBONATE, NEUTROGIN, AMIKACIN SULPHATE, LASIX, VORICONAZOLE, RABEPRAZOLE, ENALAPRIL MALEATE. Patient died on 05/07/2007.
Velcade Side Effects Report #5261520-3
Physician from JAPAN reported VELCADE problem on Feb 19, 2007. Male patient, 71 years of age, was diagnosed with multiple myeloma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: basophil count decreased, blood alkaline phosphatase decreased, blood lactate dehydrogenase increased, blood urea increased, blood uric acid increased, c-reactive protein increased, computerised tomogram thorax abnormal, febrile neutropenia, fungal dna test positive, . VELCADE dosage: 1.4 MG, INTRAVENOUS. During the same period patient was treated with ZOMETA, BICARBONATE, NEUTROGIN, AMIKACIN SULPHATE, LASIX, VORICONAZOLE, RABEPRAZOLE, ENALAPRIL MALEATE. Patient recovered.
Tysabri Side Effects Report #5599218-4
TYSABRI problem was reported by a Health Professional from UNITED STATES on Jan 04, 2008. Female patient, 28 years of age, weighting 125.0 lb, was diagnosed with multiple sclerosis and was treated with TYSABRI. After drug was administered, patient experienced the following problems/side effects: bacteria urine identified, blood albumin decreased, blood alkaline phosphatase decreased, blood urine present, colitis, culture stool positive, gastroenteritis, haematocrit decreased, haemoglobin decreased, . TYSABRI dosage: 300 MG; QM; IV. During the same period patient was treated with BACLOFEN, AMANTADINE, ORAL CONTRACEPTIVE, WELLBUTRIN, VITAMIN, BOTOX. Patient was hospitalized. Patient recovered.
Requip Side Effects Report #5529367-8
Consumer or non-health professional from UNITED STATES reported REQUIP problem on Nov 27, 2007. Male patient was diagnosed with restless legs syndrome and was treated with REQUIP. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase decreased, liver function test abnormal, . REQUIP dosage: 3MG AT NIGHT. During the same period patient was treated with FLEXERIL, MOBIC, TYLENOL, ASPIRIN, ANTIDEPRESSANT, NORCO. Patient recovered.
Fortum Side Effects Report #5443395-2
FORTUM problem was reported by a Pharmacist from FRANCE on Sept 04, 2007. Male patient, weighting 7.72 lb, was diagnosed with sepsis, pain, antifungal prophylaxis and was treated with FORTUM. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase decreased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, hepatic enzyme abnormal, transaminases increased, . FORTUM dosage: 60MG THREE TIMES PER DAY. During the same period patient was treated with AMOXICILLIN, CLAFORAN, GENTAMICIN, AMIKLIN, PARACETAMOL, VITAMINS, FUNGIZONE, CIFLOX. Patient was hospitalized. Patient recovered.
Fortum Side Effects Report #5386597-6
Pharmacist from FRANCE reported FORTUM problem on July 12, 2007. Female patient, weighting 7.72 lb, was diagnosed with sepsis and was treated with FORTUM. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase decreased, . FORTUM dosage: 60MG THREE TIMES PER DAY. During the same period patient was treated with AMOXICILLIN, CLAFORAN, GENTAMICIN, AMIKLIN, VITAMIN. Patient was hospitalized. Patient recovered.
Fortum Side Effects Report #5386597-6
FORTUM problem was reported by a Pharmacist from FRANCE on July 12, 2007. Female patient, weighting 7.72 lb, was diagnosed with sepsis and was treated with FORTUM. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase decreased, . FORTUM dosage: 60MG THREE TIMES PER DAY. During the same period patient was treated with AMOXICILLIN, CLAFORAN, GENTAMICIN, AMIKLIN, VITAMIN. Patient was hospitalized. Patient recovered.
Comtan Side Effects Report #5690136-X
Consumer or non-health professional from JAPAN reported COMTAN problem on Mar 21, 2008. Female patient, 69 years of age, was treated with COMTAN. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase decreased, gamma-glutamyltransferase increased, hepatic function abnormal, . COMTAN dosage: 100 MG, TID. During the same period patient was treated with LEVODOPA BENSERAZIDE HYDROCHLO, SYMMETREL, PERMAX. Patient recovered.
Strattera Side Effects Report #5314953-0
STRATTERA problem was reported by a Physician from UNITED STATES on Apr 18, 2007. Male patient, 15 years of age, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase decreased, blood creatinine increased, blood sodium increased, blood urea decreased, influenza like illness, . STRATTERA dosage: unknown. Patient recovered.
Strattera Side Effects Report #5338852-3
Physician from UNITED STATES reported STRATTERA problem on May 18, 2007. Male patient, 15 years of age, weighting 140.0 lb, was diagnosed with attention deficit/hyperactivity disorder and was treated with STRATTERA. After drug was administered, patient experienced the following problems/side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase decreased, blood creatinine increased, blood sodium increased, blood urea decreased, cough, fatigue, headache, . STRATTERA dosage: 40 MG, UNK. Patient recovered.