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

HAEMATOMA ( 10 FDA reports)
AMNIOTIC CAVITY DISORDER ( 8 FDA reports)
AMNIOTIC FLUID VOLUME DECREASED ( 8 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 5 FDA reports)
ABORTION INDUCED ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
ACUTE GENERALISED EXANTHEMATOUS PUSTULOSIS ( 4 FDA reports)
RENAL FAILURE ( 4 FDA reports)
METRORRHAGIA ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
SHOCK HAEMORRHAGIC ( 3 FDA reports)
RASH MACULO-PAPULAR ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PAIN IN EXTREMITY ( 3 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 3 FDA reports)
MUSCLE DISORDER ( 3 FDA reports)
CARDIO-RESPIRATORY ARREST ( 3 FDA reports)
HYPERTHERMIA ( 3 FDA reports)
CONFUSIONAL STATE ( 3 FDA reports)
DRUG INTERACTION ( 3 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
DEATH ( 2 FDA reports)
TRANSFUSION ( 2 FDA reports)
DYSPNOEA ( 2 FDA reports)
TOXIC EPIDERMAL NECROLYSIS ( 2 FDA reports)
TONGUE ULCERATION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
SOMNOLENCE ( 2 FDA reports)
SKIN LESION ( 2 FDA reports)
FACIAL BONES FRACTURE ( 2 FDA reports)
FALL ( 2 FDA reports)
FATIGUE ( 2 FDA reports)
RASH PUSTULAR ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
CONJUNCTIVITIS ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HALLUCINATION, VISUAL ( 2 FDA reports)
PYREXIA ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 2 FDA reports)
HYPERCALCAEMIA ( 2 FDA reports)
HYPERKALAEMIA ( 2 FDA reports)
PROTHROMBIN LEVEL DECREASED ( 2 FDA reports)
PLATELET COUNT DECREASED ( 2 FDA reports)
BURNING SENSATION ( 2 FDA reports)
LEUKOPENIA ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
CARDIAC FAILURE ( 2 FDA reports)
LYMPHOCYTE COUNT ABNORMAL ( 1 FDA reports)
LYMPHOPENIA ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
COMA ( 1 FDA reports)
MUCOUS MEMBRANE DISORDER ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
MUSCLE HAEMORRHAGE ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
LOCALISED OEDEMA ( 1 FDA reports)
NEUTROPHIL COUNT INCREASED ( 1 FDA reports)
NEUTROPHILIA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
OLIGOHYDRAMNIOS ( 1 FDA reports)
OVERDOSE ( 1 FDA reports)
PAIN ( 1 FDA reports)
INTERTRIGO ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
INFECTION ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
PROTHROMBIN TIME RATIO DECREASED ( 1 FDA reports)
HERPES VIRUS INFECTION ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPOPLASIA ( 1 FDA reports)
PUSTULAR PSORIASIS ( 1 FDA reports)
HERPES SIMPLEX ( 1 FDA reports)
RALES ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
FOLATE DEFICIENCY ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
FOETAL DISORDER ( 1 FDA reports)
ANTINUCLEAR ANTIBODY POSITIVE ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
EYELID OEDEMA ( 1 FDA reports)
ERYTHEMA ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
THERAPEUTIC AGENT TOXICITY ( 1 FDA reports)
ELECTROENCEPHALOGRAM ABNORMAL ( 1 FDA reports)
ECZEMA ( 1 FDA reports)
COUGH ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)

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