Please choose an event type to view the corresponding MedsFacts report:

FATIGUE ( 3 FDA reports)
SKIN LESION ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
SCIATICA ( 2 FDA reports)
RASH MACULO-PAPULAR ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
MUSCLE ABSCESS ( 2 FDA reports)
JOINT EFFUSION ( 2 FDA reports)
JOINT ABSCESS ( 2 FDA reports)
HEADACHE ( 2 FDA reports)
FEBRILE BONE MARROW APLASIA ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
DEEP VEIN THROMBOSIS ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
COAGULATION FACTOR VIII LEVEL DECREASED ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DIARRHOEA ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
BODY TEMPERATURE INCREASED ( 1 FDA reports)
EDUCATIONAL PROBLEM ( 1 FDA reports)
ELECTROCARDIOGRAM T WAVE INVERSION ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE PRURITUS ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GLOMERULONEPHRITIS MINIMAL LESION ( 1 FDA reports)
HAEMATOSPERMIA ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOAESTHESIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFUSION SITE IRRITATION ( 1 FDA reports)
INTRACRANIAL VENOUS SINUS THROMBOSIS ( 1 FDA reports)
BACTERIAL SEPSIS ( 1 FDA reports)
BACK PAIN ( 1 FDA reports)
LOWER EXTREMITY MASS ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MASS ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEPHROTIC SYNDROME ( 1 FDA reports)
NERVE COMPRESSION ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
ARTHRITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
ANTEPARTUM HAEMORRHAGE ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PREMATURE LABOUR ( 1 FDA reports)
PREMATURE SEPARATION OF PLACENTA ( 1 FDA reports)
RASH ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
RED BLOOD CELLS SEMEN ( 1 FDA reports)
REFUSAL OF TREATMENT BY RELATIVE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ABDOMINAL TENDERNESS ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPY NON-RESPONDER ( 1 FDA reports)
TREATMENT NONCOMPLIANCE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
UTERINE CONTRACTIONS ABNORMAL ( 1 FDA reports)

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