MONOCYTE PERCENTAGE INCREASED side effect
What is MONOCYTE PERCENTAGE INCREASED ?
Help Community - Describe Your Side Effect
Search FDA Side Effects
Ask Health Expert
MONOCYTE PERCENTAGE INCREASED and Recently Reported Side Effects
MONOCYTE PERCENTAGE INCREASED and 15 most Active Side Effect polls
MONOCYTE PERCENTAGE INCREASED and featured health surveys
Substances toxic to Health
Recent Hospital reviews
Comments about Side Effects
Hospital Quality reviews
Homecare Quality reviews
Raptiva Side Effects Report #5270597-0
Health Professional from UNITED STATES reported RAPTIVA problem on Mar 10, 2007. Female patient, 67 years of age, was diagnosed with psoriasis and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: monocyte percentage increased, neutrophil count decreased, . RAPTIVA dosage: 0.6 ML, 1/WEEK, SUBCUTANEOUS. 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.
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.
Diovan Side Effects Report #5763587-2
DIOVAN problem was reported by a Physician from JAPAN on May 30, 2008. Female patient, 73 years of age, was diagnosed with hypertension, diabetes mellitus, pharyngitis, gastritis and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: flushing, monocyte percentage increased, purpura, rash, skin exfoliation, thirst, . DIOVAN dosage: unknown. During the same period patient was treated with SEIBULE, LOXONIN, APLACE, GENINAX, CONIEL, CALBLOCK. Patient was hospitalized. Patient recovered.
Diovan Side Effects Report #5777331-6
Physician from JAPAN reported DIOVAN problem on June 10, 2008. Female patient was diagnosed with hypertension, diabetes mellitus, pharyngitis, gastritis and was treated with DIOVAN. After drug was administered, patient experienced the following problems/side effects: flushing, lymphocyte stimulation test positive, monocyte percentage increased, purpura, rash, skin exfoliation, thirst, . DIOVAN dosage: unknown. During the same period patient was treated with SEIBULE, LOXONIN, APLACE, GENINAX, CONIEL, CALBLOCK. Patient was hospitalized. Patient recovered.
Aromasin Side Effects Report #5706769-8
AROMASIN problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 15, 2008. Female patient, weighting 131.0 lb, was treated with AROMASIN. After drug was administered, patient experienced the following problems/side effects: agranulocytosis, lymphocyte percentage increased, monocyte percentage increased, neutropenia, white blood cell count decreased, . AROMASIN dosage: 147.5 MG. Patient was hospitalized. Patient recovered.