HAEMATOCRIT INCREASED side effect
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Drugs associated with HAEMATOCRIT INCREASED
ANDROGEL AVONEX BETASERON CETROTIDE CYCLOSPORINE DECITABINE DIUVER FLOXURIDINE FLUOROURACIL FOLLITROPIN IBUPROFEN KEPPRA LAPATINIB LYRICA NORVASC PEPCID PRIALT ROACCUTANE SUTENT TESTOGEL TESTOSTERONE TRACLEER ZYPREXANorvasc Side Effects Report #5409975-5
Physician from JAPAN reported NORVASC problem on July 31, 2007. Male patient, 57 years of age, was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, haemoglobin increased, red blood cell count increased, . NORVASC dosage: DAILY DOSE:10MG. During the same period patient was treated with AMARYL, MICARDIS, OMEPRAZOLE, MUCOSTA, WARFARIN, ANPLAG. Patient recovered.
Norvasc Side Effects Report #5401703-2
NORVASC problem was reported by a Pharmacist from JAPAN on July 19, 2007. Male patient, 57 years of age, was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, haemoglobin increased, red blood cell count increased, . NORVASC dosage: DAILY DOSE:10MG. During the same period patient was treated with AMARYL, MICARDIS, WARFARIN, OMEPRAZOLE, ANPLAG, MUCOSTA. Patient recovered.
Norvasc Side Effects Report #5401703-2
Pharmacist from JAPAN reported NORVASC problem on July 19, 2007. Male patient, 57 years of age, was treated with NORVASC. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, haemoglobin increased, red blood cell count increased, . NORVASC dosage: DAILY DOSE:10MG. During the same period patient was treated with AMARYL, MICARDIS, WARFARIN, OMEPRAZOLE, ANPLAG, MUCOSTA. Patient recovered.
Testogel Side Effects Report #5353539-9
TESTOGEL problem was reported by a Consumer or non-health professional from UNITED KINGDOM on May 30, 2007. Male patient was diagnosed with androgen deficiency, hypertension, atrial fibrillation, irritable bowel syndrome, dysuria and was treated with TESTOGEL. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, prostatic disorder, . TESTOGEL dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, WARFARIN, CODEINE SUL, ALFUZOSIN. Patient was hospitalized. Patient recovered.
Lapatinib Side Effects Report #5328690-X
Physician from GREECE reported LAPATINIB problem on May 16, 2007. Female patient, 60 years of age, weighting 154.3 lb, was diagnosed with breast cancer, myelodysplastic syndrome and was treated with LAPATINIB. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, platelet count increased, . LAPATINIB dosage: unknown. During the same period patient was treated with PERSANTIN. Patient recovered.
Lyrica Side Effects Report #5255760-7
LYRICA problem was reported by a Health Professional from UNITED STATES on Feb 21, 2007. Female patient, weighting 170.0 lb, was diagnosed with fibromyalgia and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, haemoglobin increased, orthostatic hypotension, . LYRICA dosage: unknown. During the same period patient was treated with CELEBREX, MORPHINE SULPHATE, ARTHROTEC, CYMBALTA, ZYRTEC, ASCORBIC ACID, CALCIUM. Patient recovered.
Betaseron Side Effects Report #5262962-2
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Feb 27, 2007. Female patient, 40 years of age, was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, haemoglobin decreased, joint destruction, . BETASERON dosage: unknown. Patient recovered.
Avonex Side Effects Report #5660891-3
AVONEX problem was reported by a Physician from JAPAN on Feb 22, 2008. Female patient, 36 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: asthenia, haematocrit increased, malaise, pyrexia, red blood cell count increased, . AVONEX dosage: unknown. During the same period patient was treated with METHYCOOL, CINAL, MYONAL, JUVELA NICOTINATE, DEPAS, LENDORMIN, GLYSENNID, MAGNESIUM OXIDE. Patient was hospitalized. Patient recovered.
Roaccutane Side Effects Report #5645290-2
Physician from BELGIUM reported ROACCUTANE problem on Feb 19, 2008. Male patient, 16 years of age, was diagnosed with acne and was treated with ROACCUTANE. After drug was administered, patient experienced the following problems/side effects: blood cholesterol increased, haematocrit increased, haemoglobin increased, . ROACCUTANE dosage: unknown. Patient recovered.
Avonex Side Effects Report #5586156-6
AVONEX problem was reported by a Physician from JAPAN on Dec 21, 2007. Female patient, 36 years of age, was diagnosed with relapsing-remitting multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: asthenia, haematocrit increased, malaise, pyrexia, red blood cell count increased, . AVONEX dosage: unknown. During the same period patient was treated with METHYCOOL, CINAL, MYONAL, JUVELA NICOTINATE, DEPAS, LENDORMIN. Patient was hospitalized. Patient recovered.
Betaseron Side Effects Report #5512159-3
Consumer or non-health professional from UNITED STATES reported BETASERON problem on Oct 30, 2007. Female patient, 40 years of age, was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: fracture, haematocrit increased, haemoglobin decreased, osteoporosis, . BETASERON dosage: unknown. Patient was hospitalized. Patient recovered.
Diuver Side Effects Report #5528561-X
DIUVER problem was reported by a Consumer or non-health professional from RUSSIAN FEDERATION on Nov 09, 2007. Male patient, 60 years of age, was diagnosed with cardiac failure congestive, hypertension and was treated with DIUVER. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, haemoconcentration, . DIUVER dosage: 10MG, ONCE DAILY ORAL. During the same period patient was treated with ENALAPRIL MALEATE, ENALAPRIL MALEATE, HYDROCHLOROTHIAZIDE, SPIRONOLACTONE, AMLODIPINE, DIGOXIN. Patient recovered.
Floxuridine Side Effects Report #5445732-1
Physician from UNITED STATES reported FLOXURIDINE problem on Aug 23, 2007. Female patient, 73 years of age, was diagnosed with metastases to lung and was treated with FLOXURIDINE. After drug was administered, patient experienced the following problems/side effects: dyspnoea, haematocrit increased, haemoglobin increased, pulmonary arteriovenous fistula, tachycardia, . FLOXURIDINE dosage: unknown. During the same period patient was treated with FLUOROURACIL, ALPHA, GEMCITABINE, CAPECITABINE. Patient recovered.
Prialt Side Effects Report #5397039-9
PRIALT problem was reported by a Health Professional from UNITED STATES on July 06, 2007. Female patient, 53 years of age, was diagnosed with bone pain and was treated with PRIALT. After drug was administered, patient experienced the following problems/side effects: conjunctival haemorrhage, haematocrit increased, haemoglobin increased, international normalised ratio decreased, petechiae, red blood cell count increased, . PRIALT dosage: unknown. Patient recovered.
Tracleer Side Effects Report #5401857-8
Physician from GREECE reported TRACLEER problem on July 13, 2007. Female patient, 59 years of age, was diagnosed with pulmonary hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: dysarthria, haematocrit increased, hypoaesthesia, . TRACLEER dosage: 125 MG, BID, ORAL. During the same period patient was treated with SOLOSA, AFLEN, OXYGEN. Patient recovered.
Prialt Side Effects Report #5397039-9
PRIALT problem was reported by a Health Professional from UNITED STATES on July 06, 2007. Female patient, 53 years of age, was diagnosed with bone pain and was treated with PRIALT. After drug was administered, patient experienced the following problems/side effects: conjunctival haemorrhage, haematocrit increased, haemoglobin increased, international normalised ratio decreased, petechiae, red blood cell count increased, . PRIALT dosage: unknown. Patient recovered.
Tracleer Side Effects Report #5401857-8
Physician from GREECE reported TRACLEER problem on July 13, 2007. Female patient, 59 years of age, was diagnosed with pulmonary hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: dysarthria, haematocrit increased, hypoaesthesia, . TRACLEER dosage: 125 MG, BID, ORAL. During the same period patient was treated with SOLOSA, AFLEN, OXYGEN. Patient recovered.
Sutent Side Effects Report #5735581-9
SUTENT problem was reported by a Physician from UNITED KINGDOM on Apr 30, 2008. Male patient, weighting 187.4 lb, was diagnosed with renal cancer metastatic, splenectomy and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: blood erythropoietin increased, haematocrit increased, haemoglobin increased, macrocytosis, volume blood decreased, . SUTENT dosage: unknown. During the same period patient was treated with PENICILLIN, LANSOPRAZOLE. Patient recovered.
Sutent Side Effects Report #5711779-0
Physician from UNITED KINGDOM reported SUTENT problem on Apr 09, 2008. Male patient, weighting 187.4 lb, was diagnosed with renal cancer metastatic, splenectomy and was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: blood erythropoietin increased, haematocrit increased, haemoglobin increased, macrocytosis, volume blood decreased, . SUTENT dosage: unknown. During the same period patient was treated with PENICILLIN, LANSOPRAZOLE. Patient recovered.
Prialt Side Effects Report #5363025-8
PRIALT problem was reported by a Health Professional from UNITED STATES on June 01, 2007. Female patient, 53 years of age, was diagnosed with pain and was treated with PRIALT. After drug was administered, patient experienced the following problems/side effects: erythema, haematocrit increased, haemoglobin increased, international normalised ratio decreased, ocular hyperaemia, red blood cell count increased, . PRIALT dosage: unknown. Patient recovered.
Testosterone Side Effects Report #5370033-X
Consumer or non-health professional from UNITED KINGDOM reported TESTOSTERONE problem on June 15, 2007. Male patient was diagnosed with androgen deficiency, hypertension, atrial fibrillation, irritable bowel syndrome, dysuria and was treated with TESTOSTERONE. After drug was administered, patient experienced the following problems/side effects: escherichia urinary tract infection, haematocrit increased, prostatic disorder, . TESTOSTERONE dosage: unknown. During the same period patient was treated with ENALAPRIL, WARFARIN, CODEINE SUL, ALFUZOSIN. Patient was hospitalized. Patient recovered.
Androgel Side Effects Report #5345638-2
ANDROGEL problem was reported by a Physician from UNITED STATES on Sept 18, 2006. Male patient, 57 years of age, weighting 242.5 lb, was diagnosed with hypogonadism and was treated with ANDROGEL. After drug was administered, patient experienced the following problems/side effects: benign prostatic hyperplasia, haematocrit increased, prostatic specific antigen increased, . ANDROGEL dosage: unknown. During the same period patient was treated with ACTOS, METFORMIN, AVALIDE, ASPIRIN, GLIPIZIDE, LESCOL, ZETIA, VIAGRA. Patient recovered.
Androgel Side Effects Report #5682209-2
Consumer or non-health professional from UNITED STATES reported ANDROGEL problem on Mar 13, 2008. Male patient, weighting 159.8 lb, was diagnosed with blood testosterone decreased and was treated with ANDROGEL. After drug was administered, patient experienced the following problems/side effects: amaurosis fugax, atrial fibrillation, haematocrit increased, haemoglobin increased, syncope vasovagal, tachyarrhythmia, . ANDROGEL dosage: unknown. Patient recovered.
Ibuprofen Side Effects Report #5601152-8
IBUPROFEN problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Jan 04, 2008. Female patient, child 7 years of age, was diagnosed with abdominal pain and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: dialysis, gastroenteritis, haematocrit increased, hypertension, hypovolaemia, renal failure acute, renal tubular necrosis, . IBUPROFEN dosage: (150 MG; ORAL). During the same period patient was treated with DICLOFENAC, CEFTRIAXONE. Patient was hospitalized. Patient recovered.
Fluorouracil Side Effects Report #5426009-7
Physician from UNITED STATES reported FLUOROURACIL problem on Aug 23, 2007. Female patient, weighting 136.2 lb, was diagnosed with bile duct cancer and was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: abdominal pain, ascites, haematocrit increased, paracentesis, white blood cell count increased, . FLUOROURACIL dosage: 975MG IV OVER 30 MINUTES. During the same period patient was treated with DAVANAT, ALDACTONE. Patient was hospitalized. Patient recovered.
Fluorouracil Side Effects Report #5392954-4
FLUOROURACIL problem was reported by a Consumer or non-health professional from UNITED STATES on July 04, 2007. Female patient, 73 years of age, was diagnosed with metastases to lung and was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: arteriovenous malformation, blood erythropoietin increased, haematocrit increased, haemoglobin increased, haemoptysis, metastases to lung, oxygen saturation decreased, tachycardia, . FLUOROURACIL dosage: unknown. During the same period patient was treated with INTERFERON ALFA, CAPECITABINE, GEMCITABINE, FLOXURIDINE. Patient recovered.
Floxuridine Side Effects Report #5402053-0
Health Professional from UNITED STATES reported FLOXURIDINE problem on July 17, 2007. Female patient, 73 years of age, was diagnosed with metastases to lung and was treated with FLOXURIDINE. After drug was administered, patient experienced the following problems/side effects: arteriovenous malformation, blood erythropoietin increased, haematocrit increased, haemoglobin increased, mixed venous blood saturation decreased, oxygen saturation decreased, tachycardia, . FLOXURIDINE dosage: unknown. Patient was hospitalized. Patient recovered.
Fluorouracil Side Effects Report #5392954-4
FLUOROURACIL problem was reported by a Consumer or non-health professional from UNITED STATES on July 04, 2007. Female patient, 73 years of age, was diagnosed with metastases to lung and was treated with FLUOROURACIL. After drug was administered, patient experienced the following problems/side effects: arteriovenous malformation, blood erythropoietin increased, haematocrit increased, haemoglobin increased, haemoptysis, metastases to lung, oxygen saturation decreased, tachycardia, . FLUOROURACIL dosage: unknown. During the same period patient was treated with INTERFERON ALFA, CAPECITABINE, GEMCITABINE, FLOXURIDINE. Patient recovered.
Floxuridine Side Effects Report #5402053-0
Health Professional from UNITED STATES reported FLOXURIDINE problem on July 17, 2007. Female patient, 73 years of age, was diagnosed with metastases to lung and was treated with FLOXURIDINE. After drug was administered, patient experienced the following problems/side effects: arteriovenous malformation, blood erythropoietin increased, haematocrit increased, haemoglobin increased, mixed venous blood saturation decreased, oxygen saturation decreased, tachycardia, . FLOXURIDINE dosage: unknown. Patient was hospitalized. Patient recovered.
Cyclosporine Side Effects Report #5725557-X
CYCLOSPORINE problem was reported by a Health Professional from SAUDI ARABIA on Apr 24, 2008. Male patient, 50 years of age, was diagnosed with renal transplant and was treated with CYCLOSPORINE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, complications of transplanted kidney, haematocrit increased, haemodialysis, haemoglobin increased, hydronephrosis, mean cell volume decreased, phlebotomy, polycythaemia, . CYCLOSPORINE dosage: 4 MG/KG/D. Patient recovered.
Keppra Side Effects Report #5741336-1
Consumer or non-health professional from GERMANY reported KEPPRA problem on Apr 30, 2008. Male patient was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: haematocrit increased, sepsis neonatal, . KEPPRA dosage: 2000 MG /D TRP. Patient was hospitalized. Patient recovered.
Zyprexa Side Effects Report #5692981-3
ZYPREXA problem was reported by a Physician from UNITED STATES on Mar 25, 2008. Male patient was diagnosed with agitation and was treated with ZYPREXA. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, blood urea increased, haematocrit increased, red blood cell count decreased, sedation, . ZYPREXA dosage: 10 MG, UNK. During the same period patient was treated with FERRO, PROTONIX. Patient recovered.
Cetrotide Side Effects Report #5711126-4
Consumer or non-health professional from FRANCE reported CETROTIDE problem on Apr 07, 2008. Female patient, 31 years of age, was diagnosed with in vitro fertilisation and was treated with CETROTIDE. After drug was administered, patient experienced the following problems/side effects: abdominal pain, ascites, haematocrit increased, haemoconcentration, haemoglobin increased, ovarian hyperstimulation syndrome, vomiting, weight decreased, . CETROTIDE dosage: 0.25 MG, 1 IN 1 DAYS, SUBCUTANEOUS. During the same period patient was treated with CHORIONIC GONADTROPIN, PUREGON. Patient was hospitalized. Patient recovered.
Androgel Side Effects Report #5712211-3
ANDROGEL problem was reported by a Pharmacist from UNITED STATES on Apr 16, 2008. Male patient, weighting 159.8 lb, was diagnosed with blood testosterone decreased and was treated with ANDROGEL. After drug was administered, patient experienced the following problems/side effects: amaurosis fugax, atrial fibrillation, haematocrit increased, haemoglobin increased, syncope vasovagal, tachyarrhythmia, . ANDROGEL dosage: unknown. Patient recovered.
Decitabine Side Effects Report #5717276-0
Physician from VENEZUELA reported DECITABINE problem on Apr 17, 2008. Male patient, 73 years of age, weighting 149.9 lb, was diagnosed with myelodysplastic syndrome and was treated with DECITABINE. After drug was administered, patient experienced the following problems/side effects: blood lactate dehydrogenase increased, cerebral haematoma, haematocrit increased, haemoglobin decreased, haemorrhagic stroke, hypertensive crisis, platelet count decreased, . DECITABINE dosage: 15 MG/M2, INTRAVENOUS. During the same period patient was treated with AVANDIA, DIAMICRON, FOLIC ACID, VITAMIN D, GABAPENTIN, LEVOTHYROXINE, ACETAMINOPHEN, ACYCLOVIR. Patient was hospitalized. Patient died on 02/23/2008.
Follitropin Side Effects Report #5324706-5
FOLLITROPIN ALPHA problem was reported by a Consumer or non-health professional from JAPAN on Apr 25, 2007. Female patient, 32 years of age, was diagnosed with assisted fertilisation and was treated with FOLLITROPIN ALPHA. After drug was administered, patient experienced the following problems/side effects: ascites, dyspnoea, haematocrit increased, hypovolaemic shock, ovarian enlargement, ovarian hyperstimulation syndrome, pleural effusion, . FOLLITROPIN ALPHA dosage: unknown. During the same period patient was treated with CHORIONIC GONADOTROPIN. Patient was hospitalized. Patient recovered.
Pepcid Side Effects Report #5253704-5
Health Professional from JAPAN reported PEPCID problem on Feb 19, 2007. Male patient, 54 years of age, was treated with PEPCID. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, asthenia, haematocrit increased, hypochloraemia, hypokalaemia, metabolic acidosis, nausea, nephritis interstitial, renal impairment, . PEPCID dosage: unknown. During the same period patient was treated with MOSAPRIDE CITRATE, POTASSIUM CHLORIDE AND CHLORIDE, CHLORIDE. Patient was hospitalized. Patient recovered.