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

NAUSEA ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
FATIGUE ( 3 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 2 FDA reports)
BLOOD BILIRUBIN INCREASED ( 2 FDA reports)
CHEST PAIN ( 2 FDA reports)
DECREASED APPETITE ( 2 FDA reports)
DIZZINESS ( 2 FDA reports)
INSOMNIA ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
PAIN ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
VOMITING ( 2 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABORTION INDUCED ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGORAPHOBIA ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANXIETY ( 1 FDA reports)
APHASIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
BACTERAEMIA ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BIPOLAR I DISORDER ( 1 FDA reports)
BLOOD ALBUMIN INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD PH DECREASED ( 1 FDA reports)
BLOOD PRESSURE INCREASED ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
CAESAREAN SECTION ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DEPRESSION ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG EXPOSURE BEFORE PREGNANCY ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG INEFFECTIVE ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSPHAGIA ( 1 FDA reports)
DYSPNOEA ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
HALLUCINATIONS, MIXED ( 1 FDA reports)
HEAD DEFORMITY ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HOT FLUSH ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
IRON DEFICIENCY ANAEMIA ( 1 FDA reports)
LEGAL PROBLEM ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LOCALISED INFECTION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MUSCLE SPASTICITY ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
NONSPECIFIC REACTION ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PARAESTHESIA ( 1 FDA reports)
PITTING OEDEMA ( 1 FDA reports)
PREGNANCY ( 1 FDA reports)
PURULENT DISCHARGE ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
RASH ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RENAL VEIN THROMBOSIS ( 1 FDA reports)
RETAINED PRODUCTS OF CONCEPTION ( 1 FDA reports)
SCHIZOPHRENIA ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN DISORDER ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
STAPHYLOCOCCAL INFECTION ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VAGINITIS BACTERIAL ( 1 FDA reports)
VASOCONSTRICTION ( 1 FDA reports)
VASOSPASM ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOCAL CORD DISORDER ( 1 FDA reports)
VOMITING PROJECTILE ( 1 FDA reports)
VULVOVAGINAL CANDIDIASIS ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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