LYMPHOCYTOSIS side effect
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Drugs associated with LYMPHOCYTOSIS
CLOZAPINE CLOZARIL EFFEXOR ESCITALOPRAM FOSAMAX KETODERM MABTHERA RAPTIVA REVLIMID SPRYCEL SUTENT TARGRETIN TOPAMAX XOLAIRXolair Side Effects Report #5664862-2
Consumer or non-health professional from SWITZERLAND reported XOLAIR problem on Mar 10, 2008. Female patient, 40 years of age, was diagnosed with asthma and was treated with XOLAIR. After drug was administered, patient experienced the following problems/side effects: lymphocytosis, respiratory tract infection, . XOLAIR dosage: unknown. Patient recovered.
Xolair Side Effects Report #5547807-5
XOLAIR problem was reported by a Consumer or non-health professional from SWITZERLAND on Nov 29, 2007. Female patient, 40 years of age, was diagnosed with asthma and was treated with XOLAIR. After drug was administered, patient experienced the following problems/side effects: lymphocytosis, respiratory tract infection, . XOLAIR dosage: unknown. Patient recovered.
Raptiva Side Effects Report #5447633-1
Pharmacist from UNITED STATES reported RAPTIVA problem on Sept 06, 2007. Male patient, weighting 168.4 lb, was diagnosed with psoriasis and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: lymphocytosis, neck mass, neutropenia, thrombocytopenia, . RAPTIVA dosage: 0.7 MG/KG SUBQ X 1 FROM 1MG/KG SUBQ WEEKLY 3-4 MONTHS. Patient was hospitalized. Patient recovered.
Revlimid Side Effects Report #5786844-2
REVLIMID problem was reported by a Physician from UNITED STATES on June 13, 2008. Male patient, 88 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: lymphocytosis, pancytopenia, . REVLIMID dosage: 15 MG, DAILY X 3 DAYS, ORAL; 15 MG, QOD, ORAL. During the same period patient was treated with PREDNISONE. Patient died on 05/28/1920.
Raptiva Side Effects Report #5676586-6
Physician from UNITED STATES reported RAPTIVA problem on Mar 21, 2008. Female patient was diagnosed with psoriasis and was treated with RAPTIVA. After drug was administered, patient experienced the following problems/side effects: lymphocyte morphology abnormal, lymphocytosis, . RAPTIVA dosage: unknown. Patient recovered.
Escitalopram Side Effects Report #5516900-5
ESCITALOPRAM problem was reported by a Consumer or non-health professional from FRANCE on Oct 25, 2007. Male patient, 32 years of age, was diagnosed with depression and was treated with ESCITALOPRAM. After drug was administered, patient experienced the following problems/side effects: cutaneous vasculitis, lymphocytosis, no therapeutic response, skin toxicity, . ESCITALOPRAM dosage: 10 MG QD PO. Patient recovered.
Fosamax Side Effects Report #5583321-9
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Dec 27, 2006. Female patient, 65 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: hypothyroidism, lymphocytosis, osteonecrosis, periarthritis, . FOSAMAX dosage: 70 MG/WKY/PO. Patient recovered.
Clozapine Side Effects Report #5788797-X
CLOZAPINE problem was reported by a Health Professional from FRANCE on June 17, 2008. Male patient was treated with CLOZAPINE. After drug was administered, patient experienced the following problems/side effects: chronic lymphocytic leukaemia, lymphocytosis, . CLOZAPINE dosage: unknown. During the same period patient was treated with LEPTICUR, ATARAX, THERALENE, ZOLOFT, SOLIAN, ZOLPIDEM TARTRATE. Patient recovered.
Clozaril Side Effects Report #5730114-5
Physician from UNITED KINGDOM reported CLOZARIL problem on Apr 28, 2008. Male patient, 27 years of age, was diagnosed with schizophrenia and was treated with CLOZARIL. After drug was administered, patient experienced the following problems/side effects: lymphocyte count increased, lymphocytosis, white blood cell count increased, . CLOZARIL dosage: 200MG DAILY. Patient recovered.
Topamax Side Effects Report #5253998-6
TOPAMAX problem was reported by a Physician from UNITED KINGDOM on Feb 20, 2007. Male patient, 15 years of age, was diagnosed with epilepsy and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia, lymphocytosis, neutrophil count decreased, . TOPAMAX dosage: unknown. During the same period patient was treated with VALPROATE. Patient recovered.
Topamax Side Effects Report #5258512-7
Physician from UNITED KINGDOM reported TOPAMAX problem on Feb 28, 2007. Male patient, weighting 66.14 lb, was diagnosed with epilepsy and was treated with TOPAMAX. After drug was administered, patient experienced the following problems/side effects: anaemia, lymphocytosis, neutrophil count decreased, . TOPAMAX dosage: unknown. During the same period patient was treated with VALPROATE. Patient recovered.
Targretin Side Effects Report #5277999-7
TARGRETIN problem was reported by a Physician from GERMANY on Mar 05, 2007. Male patient, 79 years of age, was diagnosed with mycosis fungoides and was treated with TARGRETIN. After drug was administered, patient experienced the following problems/side effects: hearing impaired, lymphocytosis, thrombocytopenia, . TARGRETIN dosage: 150 MG DAILY PO. Patient recovered.
Sprycel Side Effects Report #5279149-X
Health Professional from UNITED STATES reported SPRYCEL problem on Feb 22, 2007. Male patient, 60 years of age, was diagnosed with chronic myeloid leukaemia and was treated with SPRYCEL. After drug was administered, patient experienced the following problems/side effects: headache, lymphocytosis, . SPRYCEL dosage: unknown. Patient recovered.
Effexor Side Effects Report #5281945-X
EFFEXOR problem was reported by a Physician from UNITED STATES on Dec 19, 2005. Female patient, 46 years of age, was diagnosed with depression and was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: contusion, lymphocytosis, . EFFEXOR dosage: 75 MG 1X PER 1 DAY. During the same period patient was treated with PROZAC, ZOLOFT, NASONEX. Patient recovered.
Sutent Side Effects Report #5382272-2
Consumer or non-health professional from ARGENTINA reported SUTENT problem on June 27, 2007. Male patient, weighting 176.4 lb, was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: anaemia macrocytic, hypertension, lymphocytosis, palmar-plantar erythrodysaesthesia syndrome, . SUTENT dosage: unknown. During the same period patient was treated with NEURONTIN, MEPREDNISONE. Patient recovered.
Sutent Side Effects Report #5382272-2
SUTENT problem was reported by a Consumer or non-health professional from ARGENTINA on June 27, 2007. Male patient, weighting 176.4 lb, was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: anaemia macrocytic, hypertension, lymphocytosis, palmar-plantar erythrodysaesthesia syndrome, . SUTENT dosage: unknown. During the same period patient was treated with NEURONTIN, MEPREDNISONE. Patient recovered.
Mabthera Side Effects Report #5346524-4
Physician from UNITED KINGDOM reported MABTHERA problem on May 31, 2007. Male patient, 49 years of age, was treated with MABTHERA. After drug was administered, patient experienced the following problems/side effects: leukocytosis, leukopenia, lymphocytosis, pyrexia, . MABTHERA dosage: unknown. During the same period patient was treated with CORTISONE ACETATE, METHOTREXATE. Patient recovered.
Mabthera Side Effects Report #5368519-7
MABTHERA problem was reported by a Physician from UNITED KINGDOM on June 15, 2007. Female patient, weighting 178.6 lb, was diagnosed with rheumatoid arthritis and was treated with MABTHERA. After drug was administered, patient experienced the following problems/side effects: alveolitis, leukopenia, lymphocytosis, pyrexia, . MABTHERA dosage: unknown. During the same period patient was treated with CORTISONE ACETATE, METHOTREXATE, DECORTIN H. Patient was hospitalized. Patient recovered.
Sutent Side Effects Report #5370982-2
Consumer or non-health professional from ARGENTINA reported SUTENT problem on June 14, 2007. Male patient, weighting 176.4 lb, was treated with SUTENT. After drug was administered, patient experienced the following problems/side effects: anaemia macrocytic, hypertension, lymphocytosis, palmar-plantar erythrodysaesthesia syndrome, . SUTENT dosage: unknown. During the same period patient was treated with GABAPENTIN, MEPREDNISONE. Patient recovered.
Ketoderm Side Effects Report #5301707-4
KETODERM problem was reported by a Physician from on Apr 06, 2007. Male patient, 49 years of age, weighting 165.3 lb, was diagnosed with seborrhoeic dermatitis, gastrointestinal disorder, prophylaxis, hyperuricaemia and was treated with KETODERM. After drug was administered, patient experienced the following problems/side effects: burkitt's lymphoma, cytomegalovirus test positive, lymphocytosis, neutropenia, oesophagitis ulcerative, renal failure acute, tendonitis, . KETODERM dosage: unknown. During the same period patient was treated with DEBRIDAT, BACTRIM, FASTURTEC, ARACYTIN, METHOTREXATE. Patient was hospitalized. Patient recovered.