RED BLOOD CELL COUNT DECREASED side effect
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Drugs associated with RED BLOOD CELL COUNT DECREASED
ACTOS ADVAIR ALKERAN AMOXICILLIN AREDIA ARIMIDEX ARIXTRA ASPIRIN AVASTIN AVODART AVONEX BETASERON BEXXAR BLOPRESS BUSPAR CANCIDAS CARDENALIN CELEBREX CIPROFLOXACIN CLOZAPINE CRESTOR DACOGEN DECITABINE DENOSINE DIOVAN ERLOTINIB ESKAZOLE EXJADE FASLODEX FLUDARA FORTEO HEPARIN HUMIRA INEXIUM INFERGEN INTERFERON JANUVIA LAMOTRIGINE LEPONEX LETAIRIS LEXAPRO LOVENOX MALARONE NEXIUM PEGASYS PEPCID PLAVIX PROPECIA RAPTIVA REBETOL REBIF REVLIMID RIBAPAK RIBAVIRIN RISPERDAL RISPOLEPT RITUXAN SALAZOPYRINE SANDIMMUNE SANDOSTATIN SUBUTEX TAVANIC TEMODAL TEMOZOLOMIDE TRACLEER TRIQUILAR VALPROIC VIAGRA ZIDOVUDINE ZOMETA ZYPREXAInfergen Side Effects Report #5640782-4
Consumer or non-health professional from UNITED STATES reported INFERGEN problem on Feb 07, 2008. Female patient was diagnosed with hepatitis c and was treated with INFERGEN. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, treatment failure, urticaria, . INFERGEN dosage: unknown. During the same period patient was treated with RIBAVIRIN, CLARITIN, NEUPOGEN, PAROXETINE, TYLENOL EXTRA STRENGTH. Patient recovered.
Januvia Side Effects Report #5657310-X
JANUVIA problem was reported by a Health Professional from UNITED STATES on Nov 26, 2007. Female patient, 73 years of age, was diagnosed with diabetes mellitus and was treated with JANUVIA. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . JANUVIA dosage: 100 MG/DAILY/PO. During the same period patient was treated with ACTOS, METFORMIN. Patient recovered.
Zidovudine Side Effects Report #5585463-0
Consumer or non-health professional from UNITED STATES reported ZIDOVUDINE problem on Jan 04, 2008. Male patient, weighting 185.0 lb, was treated with ZIDOVUDINE. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . ZIDOVUDINE dosage: unknown. Patient was hospitalized. Patient recovered.
Revlimid Side Effects Report #5635135-9
REVLIMID problem was reported by a Health Professional from UNITED STATES on Nov 07, 2007. Female patient, 60 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . REVLIMID dosage: 20 MG, DAILY FOR 21 DAYS, ORAL ; 25 MG, DAILY FOR 21 DAYS OUT OF EVERY 28 DAYS, ORAL. Patient recovered.
Revlimid Side Effects Report #5638600-3
Health Professional from UNITED STATES reported REVLIMID problem on Nov 27, 2007. Female patient, 83 years of age, was diagnosed with myelodysplastic syndrome and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, vision blurred, . REVLIMID dosage: 5 MG, 1 IN 1 D, ORAL. Patient recovered.
Revlimid Side Effects Report #5641926-0
REVLIMID problem was reported by a Health Professional from UNITED STATES on Oct 26, 2007. Male patient, 79 years of age, weighting 165.0 lb, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . REVLIMID dosage: 5 MG, 1 IN 1 D, ORAL. Patient was hospitalized. Patient recovered.
Revlimid Side Effects Report #5643326-6
Pharmacist from UNITED STATES reported REVLIMID problem on Dec 18, 2007. Female patient, 78 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . REVLIMID dosage: 10 MG, QD DAYS 1/21, Q 28 DAYS. Patient recovered.
Revlimid Side Effects Report #5645863-7
REVLIMID problem was reported by a Pharmacist from UNITED STATES on Dec 12, 2007. Female patient, 65 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . REVLIMID dosage: 25 MG, DAILY FOR 21 DAYS, ORAL. Patient recovered.
Revlimid Side Effects Report #5646639-7
Health Professional from UNITED STATES reported REVLIMID problem on Nov 28, 2007. Female patient, 80 years of age, was diagnosed with myelodysplastic syndrome and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . REVLIMID dosage: 10 MG, DAILY FOR 21 DAYS, THEN OFF 7 DAYS, ORAL. Patient recovered.
Revlimid Side Effects Report #5647632-0
REVLIMID problem was reported by a Health Professional from UNITED STATES on Dec 20, 2007. Female patient, 52 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, stomatitis, . REVLIMID dosage: 25 MG, DAILY X 21 DAYS, ORAL. Patient recovered.
Raptiva Side Effects Report #5601401-6
Health Professional from UNITED STATES reported RAPTIVA problem on June 25, 2007. Female patient, 25 years of age, weighting 254.9 lb, was diagnosed with psoriasis and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . RAPTIVA dosage: 110 MG, 1/WEEK, SUBCUTANEOUS. During the same period patient was treated with PREDNISONE, MUSCLE RELAXANT. Patient recovered.
Interferon Side Effects Report #5472119-8
INTERFERON ALFACON problem was reported by a Health Professional from UNITED STATES on Sept 11, 2007. Female patient, 47 years of age, was diagnosed with hepatitis c and was treated with INTERFERON ALFACON. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . INTERFERON ALFACON dosage: unknown. During the same period patient was treated with RIBAVIRIN, IMODIUM, ULTRAM, SEROQUEL, ELAVIL. Patient recovered.
Ribapak Side Effects Report #5386405-3
Health Professional from UNITED STATES reported RIBAPAK problem on July 10, 2007. Female patient, 56 years of age, weighting 210.0 lb, was diagnosed with hepatitis c and was treated with RIBAPAK. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . RIBAPAK dosage: 1200MG QD PO. Patient recovered.
Celebrex Side Effects Report #5417155-2
CELEBREX problem was reported by a Consumer or non-health professional from UNITED STATES on May 16, 2007. Female patient, 68 years of age, weighting 210.4 lb, was diagnosed with arthralgia and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . CELEBREX dosage: 200 MG (200 MG, 1 IN 1D). During the same period patient was treated with SYNTHROID, LIPITOR. Patient recovered.
Ribapak Side Effects Report #5386405-3
Health Professional from UNITED STATES reported RIBAPAK problem on July 10, 2007. Female patient, 56 years of age, weighting 210.0 lb, was diagnosed with hepatitis c and was treated with RIBAPAK. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . RIBAPAK dosage: 1200MG QD PO. Patient recovered.
Celebrex Side Effects Report #5417155-2
CELEBREX problem was reported by a Consumer or non-health professional from UNITED STATES on May 16, 2007. Female patient, 68 years of age, weighting 210.4 lb, was diagnosed with arthralgia and was treated with CELEBREX. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . CELEBREX dosage: 200 MG (200 MG, 1 IN 1D). During the same period patient was treated with SYNTHROID, LIPITOR. Patient recovered.
Subutex Side Effects Report #5756640-0
Physician from GERMANY reported SUBUTEX problem on May 30, 2008. Male patient, 43 years of age, weighting 123.5 lb, was treated with SUBUTEX. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, weight decreased, white blood cell count decreased, . SUBUTEX dosage: unknown. Patient recovered.
Cardenalin Side Effects Report #5691018-X
CARDENALIN problem was reported by a Pharmacist from JAPAN on Mar 21, 2008. Female patient, 78 years of age, was diagnosed with hypertension and was treated with CARDENALIN. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . CARDENALIN dosage: unknown. During the same period patient was treated with TRICHLORMETHIAZIDE, ANTIHYPERTENSIVES, DILTIAZEM HYDROCHLORIDE. Patient recovered.
Pegasys Side Effects Report #5302877-4
Health Professional from UNITED STATES reported PEGASYS problem on Apr 19, 2007. Male patient, 54 years of age, weighting 185.0 lb, was diagnosed with hepatitis c and was treated with PEGASYS. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . PEGASYS dosage: unknown. During the same period patient was treated with RIBAVIRIN. Patient recovered.
Pepcid Side Effects Report #5260769-3
PEPCID problem was reported by a Physician from JAPAN on Feb 28, 2007. Female patient, 70 years of age, was treated with PEPCID. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . PEPCID dosage: unknown. Patient recovered.
Pepcid Side Effects Report #5273233-2
Physician from JAPAN reported PEPCID problem on Mar 16, 2007. Female patient, 70 years of age, was treated with PEPCID. After drug was administered, patient experienced the following problems/side effects: red blood cell count decreased, . PEPCID dosage: unknown. Patient recovered.
Crestor Side Effects Report #5647352-2
CRESTOR problem was reported by a Physician from JAPAN on Feb 27, 2008. Male patient, 67 years of age, was diagnosed with hypercholesterolaemia and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: hepatic function abnormal, red blood cell count decreased, . CRESTOR dosage: unknown. During the same period patient was treated with NORVASC. Patient recovered.
Forteo Side Effects Report #5653638-8
Consumer or non-health professional from FRANCE reported FORTEO problem on Feb 28, 2008. Female patient, 84 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: arthropathy, red blood cell count decreased, . FORTEO dosage: unknown. Patient recovered.
Heparin Side Effects Report #5661460-1
HEPARIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 04, 2008. Male patient, 62 years of age, was diagnosed with prophylaxis and was treated with HEPARIN. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, red blood cell count decreased, . HEPARIN dosage: unknown. Patient was hospitalized. Patient recovered.
Humira Side Effects Report #5667660-9
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Jan 30, 2008. Female patient, weighting 165.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: mean cell haemoglobin, red blood cell count decreased, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE, METHOTREXATE, NABUMETONE. Patient recovered.
Advair Side Effects Report #5674664-9
ADVAIR DISKUS problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 17, 2008. Female patient, child 10 years of age, was diagnosed with bronchitis and was treated with ADVAIR DISKUS. After drug was administered, patient experienced the following problems/side effects: hypoglycaemia, red blood cell count decreased, . ADVAIR DISKUS dosage: unknown. During the same period patient was treated with BENZONATATE, OMEPRAZOLE, AMLODIPINE, ASPIRIN. Patient recovered.
Valproic Side Effects Report #5674953-8
Consumer or non-health professional from UNITED STATES reported VALPROIC ACID problem on Mar 10, 2008. Male patient, 16 years of age, weighting 129.4 lb, was diagnosed with convulsion and was treated with VALPROIC ACID. After drug was administered, patient experienced the following problems/side effects: neutropenia, red blood cell count decreased, . VALPROIC ACID dosage: unknown. During the same period patient was treated with VALPROIC ACID, CLONAZEPAM, ACETAZOLAMIDE. Patient was hospitalized. Patient recovered.
Aspirin Side Effects Report #5676978-5
ASPIRIN problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 10, 2008. Male patient was diagnosed with cardiovascular event prophylaxis and was treated with ASPIRIN. After drug was administered, patient experienced the following problems/side effects: erosive oesophagitis, red blood cell count decreased, thrombosis, . ASPIRIN dosage: TOTAL DAILY DOSE: 81 MG UNIT DOSE: 81 MG. Patient recovered.
Avonex Side Effects Report #5681066-8
Physician from UNITED STATES reported AVONEX problem on Mar 12, 2008. Female patient, 41 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: bone marrow failure, red blood cell count decreased, thrombocytopenia, white blood cell count decreased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Cancidas Side Effects Report #5622080-8
CANCIDAS problem was reported by a Physician from SPAIN on Feb 04, 2008. Male patient, 68 years of age, was diagnosed with candidiasis and was treated with CANCIDAS. After drug was administered, patient experienced the following problems/side effects: platelet count decreased, red blood cell count decreased, white blood cell count decreased, . CANCIDAS dosage: unknown. Patient recovered.
Crestor Side Effects Report #5624486-X
Physician from JAPAN reported CRESTOR problem on Feb 04, 2008. Male patient, 67 years of age, was diagnosed with hypercholesterolaemia and was treated with CRESTOR. After drug was administered, patient experienced the following problems/side effects: hepatic function abnormal, red blood cell count decreased, . CRESTOR dosage: unknown. During the same period patient was treated with NORVASC. Patient recovered.
Revlimid Side Effects Report #5637811-0
REVLIMID problem was reported by a Physician from UNITED STATES on Feb 11, 2008. Male patient, 74 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: chronic lymphocytic leukaemia, red blood cell count decreased, . REVLIMID dosage: unknown. Patient was hospitalized. Patient recovered.
Revlimid Side Effects Report #5638181-4
Health Professional from UNITED STATES reported REVLIMID problem on Nov 28, 2007. Female patient, 61 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: fatigue, red blood cell count decreased, . REVLIMID dosage: 10 MG, DAILY X 21 DAYS, ORAL. Patient recovered.
Revlimid Side Effects Report #5638365-5
REVLIMID problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 19, 2007. Male patient was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: haematocrit decreased, red blood cell count decreased, . REVLIMID dosage: 25 MG, DAILY, ORAL. Patient recovered.
Revlimid Side Effects Report #5639175-5
Health Professional from UNITED STATES reported REVLIMID problem on Oct 17, 2007. Male patient, 56 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: dyspnoea, red blood cell count decreased, thrombosis, white blood cell count decreased, . REVLIMID dosage: 20 MG, X21 DAYS EVERY 28 DAYS, ORAL. Patient recovered.
Revlimid Side Effects Report #5639185-8
REVLIMID problem was reported by a Physician from UNITED STATES on Nov 15, 2007. Male patient was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: disease progression, red blood cell count decreased, white blood cell count decreased, . REVLIMID dosage: 15 MG, 1 IN 1 D, ORAL ; 10 MG, 1 IN 1 D, ORAL. Patient recovered.
Revlimid Side Effects Report #5639586-8
Health Professional from UNITED STATES reported REVLIMID problem on Nov 13, 2007. Female patient, 82 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: platelet count decreased, red blood cell count decreased, . REVLIMID dosage: 10 MG, 1 IN 1 D, ORAL. Patient was hospitalized. Patient recovered.
Revlimid Side Effects Report #5639666-7
REVLIMID problem was reported by a Health Professional from UNITED STATES on Nov 01, 2007. Male patient, 68 years of age, was diagnosed with myelodysplastic syndrome and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased, red blood cell count decreased, . REVLIMID dosage: 5 MG, 1 IN 1 D, ORAL. Patient recovered.
Revlimid Side Effects Report #5643467-3
Health Professional from UNITED STATES reported REVLIMID problem on Dec 18, 2007. Male patient, 64 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: cerebrovascular accident, red blood cell count decreased, . REVLIMID dosage: 25 MG, DAILY FOR 231 DAYS, ORAL. Patient was hospitalized. Patient recovered.
Revlimid Side Effects Report #5643857-9
REVLIMID problem was reported by a Health Professional from UNITED STATES on Oct 11, 2007. Male patient, 61 years of age, was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: platelet count decreased, red blood cell count decreased, . REVLIMID dosage: 25 MG, OD X 3WK, ORAL 10 MG, OD, 3 TIMES PER WEEK, ORAL. Patient recovered.
Revlimid Side Effects Report #5644001-4
Health Professional from UNITED STATES reported REVLIMID problem on Nov 15, 2007. Male patient, 44 years of age, was diagnosed with myelodysplastic syndrome and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: platelet count decreased, red blood cell count decreased, . REVLIMID dosage: 5, 10 MG, 1 IN 1 D, ORAL. Patient recovered.
Revlimid Side Effects Report #5644038-5
REVLIMID problem was reported by a Health Professional from UNITED STATES on Nov 20, 2007. Female patient, 68 years of age, was diagnosed with multiple myeloma and was treated with REVLIMID. After drug was administered, patient experienced the following problems/side effects: platelet count decreased, red blood cell count decreased, . REVLIMID dosage: 20 MG, 2 IN 1 D, ORAL. Patient was hospitalized. Patient recovered.
Rebif Side Effects Report #5564792-0
Consumer or non-health professional from GREECE reported REBIF problem on Nov 27, 2007. Female patient, 58 years of age, was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: platelet count decreased, red blood cell count decreased, white blood cell count decreased, . REBIF dosage: unknown. Patient was hospitalized. Patient recovered.
Lamotrigine Side Effects Report #5567890-0
LAMOTRIGINE problem was reported by a Pharmacist from UNITED STATES on Dec 18, 2007. Male patient, 50 years of age, weighting 220.0 lb, was treated with LAMOTRIGINE. After drug was administered, patient experienced the following problems/side effects: platelet count decreased, red blood cell count decreased, white blood cell count decreased, . LAMOTRIGINE dosage: 200MG BID PO. During the same period patient was treated with HALOPERIDOL, KEPPRA, OLANZAPINE, ASPIRIN, LANTUS, LISPRO. Patient recovered.
Dacogen Side Effects Report #5572705-0
Consumer or non-health professional from UNITED STATES reported DACOGEN problem on Aug 20, 2007. Female patient, 72 years of age, was diagnosed with leukaemia, myelodysplastic syndrome and was treated with DACOGEN. After drug was administered, patient experienced the following problems/side effects: anorexia, red blood cell count decreased, weight decreased, white blood cell count decreased, . DACOGEN dosage: unknown. Patient recovered.
Buspar Side Effects Report #5492854-5
BUSPAR problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 15, 2007. Female patient, 81 years of age, was treated with BUSPAR. After drug was administered, patient experienced the following problems/side effects: hypertension, red blood cell count decreased, renal failure, . BUSPAR dosage: unknown. During the same period patient was treated with BENAZEPRIL, HYDROCHLOROTHIAZIDE, NORVASC. Patient recovered.
Diovan Side Effects Report #5442998-9
Consumer or non-health professional from ARGENTINA reported DIOVAN problem on Aug 24, 2007. Female patient, 66 years of age, was diagnosed with hypertension and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: hyperkalaemia, red blood cell count decreased, . DIOVAN dosage: unknown. Patient was hospitalized. Patient recovered.
Viagra Side Effects Report #5450342-6
VIAGRA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 31, 2007. Male patient, weighting 170.4 lb, was diagnosed with erectile dysfunction and was treated with VIAGRA. After drug was administered, patient experienced the following problems/side effects: platelet count decreased, red blood cell count decreased, . VIAGRA dosage: TEXT:50MG PRN. Patient recovered.
Amoxicillin Side Effects Report #5459517-3
Pharmacist from JAPAN reported AMOXICILLIN TRIHYDRATE problem on Sept 18, 2007. Female patient, 58 years of age, was treated with AMOXICILLIN TRIHYDRATE. After drug was administered, patient experienced the following problems/side effects: pseudomembranous colitis, red blood cell count decreased, white blood cell count decreased, . AMOXICILLIN TRIHYDRATE dosage: 500MG PER DAY. During the same period patient was treated with FLAGYL, CALTAN, ALFAROL, DIOVAN, CALBLOCK. Patient was hospitalized. Patient recovered.
Leponex Side Effects Report #5463983-7
LEPONEX problem was reported by a Physician from SPAIN on Sept 13, 2007. Male patient, 45 years of age, was diagnosed with psychotic disorder, hepatitis c and was treated with LEPONEX. After drug was administered, patient experienced the following problems/side effects: feeling abnormal, red blood cell count decreased, white blood cell count decreased, . LEPONEX dosage: 25 MG, UNK. During the same period patient was treated with INTERFERON. Patient recovered.
Malarone Side Effects Report #5403989-7
Pharmacist from UNITED KINGDOM reported MALARONE problem on July 25, 2007. Male patient was diagnosed with malaria prophylaxis and was treated with MALARONE. After drug was administered, patient experienced the following problems/side effects: haematocrit decreased, red blood cell count decreased, thrombocytopenia, . MALARONE dosage: unknown. Patient recovered.