Adalat and platelet count decreased Patient Reports February 13, 2012

Adalat Side Effects Report #5406407-8
Adalat side effect was reported by a Pharmacist from JAPAN on July 27, 2007. Male patient, 79 years of age, weighting 110.2 lb, was diagnosed with hypertension and was treated with Adalat. After drug was administered, patient experienced the following side effects: haemorrhagic disorder, platelet count decreased. Adalat dosage: TOTAL DAILY DOSE: 40 MG UNIT DOSE: 20 MG. During the same period patient was treated with FAMOTIDINE. Patient recovered.

Adalat Side Effects Report #5692964-3
Adalat side effect was reported by a Pharmacist from JAPAN on Mar 31, 2008. Male patient, 79 years of age, weighting 110.2 lb, was diagnosed with hypertension and was treated with Adalat. After drug was administered, patient experienced the following side effects: haemorrhagic disorder, platelet count decreased. Adalat dosage: TOTAL DAILY DOSE: 40 MG UNIT DOSE: 20 MG. During the same period patient was treated with GASTER D. Patient recovered.

Adalat Side Effects Report #5695684-4
Adalat side effect was reported by a Physician from JAPAN on Mar 28, 2008. Female patient, 67 years of age, was diagnosed with hypertension and was treated with Adalat. After drug was administered, patient experienced the following side effects: platelet count decreased, rash . Adalat dosage: unknown. During the same period patient was treated with EPOGIN, NORVASC, OLMESARTAN MEDOXOMIL, ALFAROL, LASIX, NITRODERM, POTASSIUM L. Patient was hospitalized. Patient recovered.

Adalat Side Effects Report #5756664-3
Adalat side effect was reported by a Physician from JAPAN on May 26, 2008. Female patient, 67 years of age, was diagnosed with hypertension, osteoporosis , oedema, angina pectoris, hypokalaemia and was treated with Adalat. After drug was administered, patient experienced the following side effects: petechiae, platelet count decreased, renal failure chronic. Adalat dosage: unknown. During the same period patient was treated with ALFAROL, LASIX, NITRODERM, POTASSIUM L. Patient was hospitalized. Patient recovered.


Adalat Side Effects Report #5670283-9
Adalat side effect was reported by a Physician from JAPAN on Mar 11, 2008. Male patient was diagnosed with hypertension and was treated with Adalat. After drug was administered, patient experienced the following side effects: platelet count decreased, white blood cell count decreased. Adalat dosage: TOTAL DAILY DOSE: 40 MG UNIT DOSE: 20 MG. During the same period patient was treated with ATELEC. Patient recovered.

Adalat Side Effects Report #5371708-9
Adalat side effect was reported by a Pharmacist from JAPAN on June 22, 2007. Male patient was treated with Adalat. After drug was administered, patient experienced the following side effects: platelet count decreased. Adalat dosage: TOTAL DAILY DOSE: 40 MG UNIT DOSE: 20 MG. During the same period patient was treated with GASTER D, PREDONINE. Patient was hospitalized. Patient recovered.

Adalat Side Effects Report #5690043-2
Adalat side effect was reported by a Pharmacist from JAPAN on Mar 27, 2008. Female patient was treated with Adalat. After drug was administered, patient experienced the following side effects: haemoglobin decreased, platelet count decreased. Adalat dosage: TOTAL DAILY DOSE: 20 MG UNIT DOSE: 10 MG. Patient recovered.

Adalat Side Effects Report #5717432-1
Adalat side effect was reported by a Pharmacist from JAPAN on Apr 17, 2008. Female patient was treated with Adalat. After drug was administered, patient experienced the following side effects: anaemia, platelet count decreased. Adalat dosage: TOTAL DAILY DOSE: 20 MG UNIT DOSE: 10 MG. During the same period patient was treated with BIOFERMIN, MUCOSTA, MAGLAX, LAXOBERON. Patient recovered.

Adalat Side Effects Report #5753131-8
Adalat side effect was reported by a Pharmacist from JAPAN on May 23, 2008. Female patient was treated with Adalat. After drug was administered, patient experienced the following side effects: anaemia, platelet count decreased. Adalat dosage: TOTAL DAILY DOSE: 20 MG UNIT DOSE: 10 MG. During the same period patient was treated with MUCOSTA, GENTACIN, RASENAZOLIN, KEFPOLIN, LOXONIN, BIOFERMIN, MAGLAX, LAXOBERON. Patient recovered.